Linked Data
dbSNP Id:
rs1291994144
gnomAD v2:
9-93654677-C-G
gnomAD v3:
9-90892395-C-G
gnomAD v4:
9-90892395-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.90892395C>G , CM000671.2:g.90892395C>G | GRCh38 |
| NC_000009.11:g.93654677C>G , CM000671.1:g.93654677C>G | GRCh37 |
| NC_000009.10:g.92694498C>G | NCBI36 |
| NG_017046.1:g.95666C>G | |
| NG_017046.2:g.95666C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375754.9:c.1836-3133C>G MANE Select | ENSP00000364907.4:n.1836-3133C>G | |
| ENST00000375746.1:c.1836-3133C>G | ENSP00000364898.1:n.1836-3133C>G | |
| ENST00000375747.5:c.1767-3133C>G | ENSP00000364899.1:n.1767-3133C>G | |
| ENST00000375751.8:c.1767-3133C>G | ENSP00000364904.4:n.1767-3133C>G | |
| ENST00000375754.8:c.1836-3133C>G | ENSP00000364907.4:n.1836-3133C>G | |
| NM_001135052.3:c.1767-3133C>G | NP_001128524.1:n.1767-3133C>G | |
| NM_001174167.2:c.1836-3133C>G | NP_001167638.1:n.1836-3133C>G | |
| NM_001174168.2:c.1767-3133C>G | NP_001167639.1:n.1767-3133C>G | |
| NM_003177.6:c.1836-3133C>G | NP_003168.2:n.1836-3133C>G | |
| XM_005252147.2:c.1836-3133C>G | XP_005252204.1:n.1836-3133C>G | |
| XM_011518946.1:c.1836-3133C>G | XP_011517248.1:n.1836-3133C>G | |
| XM_011518947.1:c.1767-3133C>G | XP_011517249.1:n.1767-3133C>G | |
| XM_005252147.4:c.1836-3133C>G | XP_005252204.1:n.1836-3133C>G | |
| XM_011518946.3:c.1836-3133C>G | XP_011517248.1:n.1836-3133C>G | |
| XR_001746370.2:n.2039-3133C>G | ||
| NM_003177.7:c.1836-3133C>G MANE Select | NP_003168.2:n.1836-3133C>G | |
| NM_001135052.4:c.1767-3133C>G | NP_001128524.1:n.1767-3133C>G | |
| NM_001174167.3:c.1836-3133C>G | NP_001167638.1:n.1836-3133C>G | |
| NM_001174168.3:c.1767-3133C>G | NP_001167639.1:n.1767-3133C>G |