Linked Data
ClinVar Variation Id:
513632
ClinVar RCV Id:
RCV001712664
dbSNP Id:
rs138518548
ExAC:
12:15813660 G / A
gnomAD v2:
12-15813660-G-A
gnomAD v3:
12-15660726-G-A
gnomAD v4:
12-15660726-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.15660726G>A , CM000674.2:g.15660726G>A | GRCh38 |
| NC_000012.11:g.15813660G>A , CM000674.1:g.15813660G>A | GRCh37 |
| NC_000012.10:g.15704927G>A | NCBI36 |
| NG_041808.1:g.133851C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281172.10:c.825C>T MANE Select | ENSP00000281172.5:p.His275= | |
| ENST00000642278.1:c.825C>T | ENSP00000494689.1:p.His275= | |
| ENST00000642939.1:c.876C>T | ENSP00000495312.1:p.His292= | |
| ENST00000644374.1:c.825C>T | ENSP00000495956.1:p.His275= | |
| ENST00000645775.1:c.825C>T | ENSP00000495824.1:p.His275= | |
| ENST00000646123.1:c.825C>T | ENSP00000494338.1:p.His275= | |
| ENST00000646828.1:c.825C>T | ENSP00000494842.1:p.His275= | |
| ENST00000646918.1:c.825C>T | ENSP00000495722.1:p.His275= | |
| ENST00000647087.1:c.825C>T | ENSP00000496406.1:p.His275= | |
| ENST00000647224.1:c.825C>T | ENSP00000496516.1:p.His275= | |
| ENST00000281172.9:c.825C>T | ENSP00000281172.5:p.His275= | |
| ENST00000535734.5:n.105C>T | ||
| ENST00000540613.5:c.45C>T | ENSP00000441888.1:p.His15= | |
| ENST00000542903.1:c.45C>T | ENSP00000437806.1:p.His15= | |
| ENST00000543468.5:c.*85C>T | ENSP00000445985.1:n.*85C>T | |
| ENST00000543523.5:c.825C>T | ENSP00000441867.1:p.His275= | |
| ENST00000543612.5:c.825C>T | ENSP00000442388.1:p.His275= | |
| ENST00000546261.1:c.376C>T | ||
| NM_004447.5:c.825C>T | NP_004438.3:p.His275= | |
| XM_005253339.1:c.858C>T | XP_005253396.1:p.His286= | |
| XM_005253340.1:c.825C>T | XP_005253397.1:p.His275= | |
| XM_006719057.1:c.825C>T | XP_006719120.1:p.His275= | |
| XM_011520605.1:c.885C>T | XP_011518907.1:p.His295= | |
| XM_011520606.1:c.825C>T | XP_011518908.1:p.His275= | |
| XM_011520605.3:c.885C>T | XP_011518907.1:p.His295= | |
| XM_024448878.1:c.858C>T | XP_024304646.1:p.His286= | |
| XM_024448879.1:c.825C>T | XP_024304647.1:p.His275= | |
| XM_024448880.1:c.825C>T | XP_024304648.1:p.His275= | |
| XM_024448881.1:c.825C>T | XP_024304649.1:p.His275= | |
| XM_024448882.1:c.825C>T | XP_024304650.1:p.His275= | |
| NM_004447.6:c.825C>T MANE Select | NP_004438.3:p.His275= |