Linked Data
ClinVar Variation Id:
282513
dbSNP Id:
rs777216777
ExAC:
2:71886164 G / T
gnomAD v2:
2-71886164-G-T
gnomAD v3:
2-71659034-G-T
gnomAD v4:
2-71659034-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71659034G>T , CM000664.2:g.71659034G>T | GRCh38 |
| NC_000002.11:g.71886164G>T , CM000664.1:g.71886164G>T | GRCh37 |
| NC_000002.10:g.71739672G>T | NCBI36 |
| NG_008694.1:g.210412G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2325+1G>T | ENSP00000513536.1:n.2325+1G>T | |
| ENST00000698058.1:c.1542+1G>T | ENSP00000513537.1:n.1542+1G>T | |
| ENST00000698059.1:c.1650+1G>T | ENSP00000513538.1:n.1650+1G>T | |
| ENST00000258104.8:c.4794+1G>T MANE Plus Clinical | ENSP00000258104.3:n.4794+1G>T | |
| ENST00000410020.8:c.4911+1G>T MANE Select | ENSP00000386881.3:n.4911+1G>T | |
| ENST00000258104.7:c.4794+1G>T | ENSP00000258104.3:n.4794+1G>T | |
| ENST00000394120.6:c.4797+1G>T | ENSP00000377678.2:n.4797+1G>T | |
| ENST00000409366.5:c.4860+1G>T | ENSP00000386512.1:n.4860+1G>T | |
| ENST00000409582.7:c.4908+1G>T | ENSP00000386547.3:n.4908+1G>T | |
| ENST00000409651.5:c.4890+1G>T | ENSP00000386683.1:n.4890+1G>T | |
| ENST00000409744.5:c.4818+1G>T | ENSP00000386285.1:n.4818+1G>T | |
| ENST00000409762.5:c.4845+1G>T | ENSP00000387137.1:n.4845+1G>T | |
| ENST00000410020.7:c.4911+1G>T | ENSP00000386881.3:n.4911+1G>T | |
| ENST00000410041.1:c.4848+1G>T | ENSP00000386617.1:n.4848+1G>T | |
| ENST00000413539.6:c.4887+1G>T | ENSP00000407046.2:n.4887+1G>T | |
| ENST00000429174.6:c.4857+1G>T | ENSP00000398305.2:n.4857+1G>T | |
| ENST00000479049.6:n.1679+1G>T | ||
| NM_001130455.1:c.4797+1G>T | NP_001123927.1:n.4797+1G>T | |
| NM_001130976.1:c.4752+1G>T | NP_001124448.1:n.4752+1G>T | |
| NM_001130977.1:c.4815+1G>T | NP_001124449.1:n.4815+1G>T | |
| NM_001130978.1:c.4857+1G>T | NP_001124450.1:n.4857+1G>T | |
| NM_001130979.1:c.4887+1G>T | NP_001124451.1:n.4887+1G>T | |
| NM_001130980.1:c.4845+1G>T | NP_001124452.1:n.4845+1G>T | |
| NM_001130981.1:c.4908+1G>T | NP_001124453.1:n.4908+1G>T | |
| NM_001130982.1:c.4890+1G>T | NP_001124454.1:n.4890+1G>T | |
| NM_001130983.1:c.4860+1G>T | NP_001124455.1:n.4860+1G>T | |
| NM_001130984.1:c.4818+1G>T | NP_001124456.1:n.4818+1G>T | |
| NM_001130985.1:c.4848+1G>T | NP_001124457.1:n.4848+1G>T | |
| NM_001130986.1:c.4755+1G>T | NP_001124458.1:n.4755+1G>T | |
| NM_001130987.1:c.4911+1G>T | NP_001124459.1:n.4911+1G>T | |
| NM_003494.3:c.4794+1G>T | NP_003485.1:n.4794+1G>T | |
| XM_005264584.3:c.4953+1G>T | XP_005264641.1:n.4953+1G>T | |
| XM_005264585.3:c.4950+1G>T | XP_005264642.1:n.4950+1G>T | |
| XM_005264584.4:c.4953+1G>T | XP_005264641.1:n.4953+1G>T | |
| XM_005264585.5:c.4950+1G>T | XP_005264642.1:n.4950+1G>T | |
| XR_001738969.1:n.5111+1G>T | ||
| NM_001130987.2:c.4911+1G>T MANE Select | NP_001124459.1:n.4911+1G>T | |
| NM_001130455.2:c.4797+1G>T | NP_001123927.1:n.4797+1G>T | |
| NM_001130976.2:c.4752+1G>T | NP_001124448.1:n.4752+1G>T | |
| NM_001130977.2:c.4815+1G>T | NP_001124449.1:n.4815+1G>T | |
| NM_001130978.2:c.4857+1G>T | NP_001124450.1:n.4857+1G>T | |
| NM_001130979.2:c.4887+1G>T | NP_001124451.1:n.4887+1G>T | |
| NM_001130980.2:c.4845+1G>T | NP_001124452.1:n.4845+1G>T | |
| NM_001130981.2:c.4908+1G>T | NP_001124453.1:n.4908+1G>T | |
| NM_001130982.2:c.4890+1G>T | NP_001124454.1:n.4890+1G>T | |
| NM_001130983.2:c.4860+1G>T | NP_001124455.1:n.4860+1G>T | |
| NM_001130984.2:c.4818+1G>T | NP_001124456.1:n.4818+1G>T | |
| NM_001130985.2:c.4848+1G>T | NP_001124457.1:n.4848+1G>T | |
| NM_001130986.2:c.4755+1G>T | NP_001124458.1:n.4755+1G>T | |
| NM_003494.4:c.4794+1G>T MANE Plus Clinical | NP_003485.1:n.4794+1G>T |