Linked Data
ClinVar Variation Id:
749173
ClinVar RCV Id:
RCV000926022
dbSNP Id:
rs369446956
ExAC:
4:104106974 G / A
gnomAD v2:
4-104106974-G-A
gnomAD v3:
4-103185817-G-A
gnomAD v4:
4-103185817-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.103185817G>A , CM000666.2:g.103185817G>A | GRCh38 |
| NC_000004.11:g.104106974G>A , CM000666.1:g.104106974G>A | GRCh37 |
| NC_000004.10:g.104326423G>A | NCBI36 |
| NG_041798.1:g.17593C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265148.9:c.738C>T MANE Select | ENSP00000265148.3:p.Gly246= | |
| ENST00000380026.8:c.738C>T | ENSP00000369365.3:p.Gly246= | |
| ENST00000265148.7:c.738C>T | ENSP00000265148.3:p.Gly246= | |
| ENST00000380026.7:c.738C>T | ENSP00000369365.3:p.Gly246= | |
| ENST00000503705.5:c.738C>T | ENSP00000423981.1:p.Gly246= | |
| ENST00000611174.4:c.738C>T | ENSP00000483542.1:p.Gly246= | |
| NM_001286734.1:c.738C>T | NP_001273663.1:p.Gly246= | |
| NM_001813.2:c.738C>T | NP_001804.2:p.Gly246= | |
| XM_011531544.1:c.738C>T | XP_011529846.1:p.Gly246= | |
| XM_011531545.1:c.738C>T | XP_011529847.1:p.Gly246= | |
| XM_011531546.1:c.738C>T | XP_011529848.1:p.Gly246= | |
| XM_011531547.1:c.738C>T | XP_011529849.1:p.Gly246= | |
| XM_011531548.1:c.738C>T | XP_011529850.1:p.Gly246= | |
| XM_011531549.1:c.738C>T | XP_011529851.1:p.Gly246= | |
| XM_011531544.2:c.738C>T | XP_011529846.1:p.Gly246= | |
| XM_011531545.2:c.738C>T | XP_011529847.1:p.Gly246= | |
| XM_011531546.3:c.738C>T | XP_011529848.1:p.Gly246= | |
| XM_011531547.2:c.738C>T | XP_011529849.1:p.Gly246= | |
| XM_011531548.2:c.738C>T | XP_011529850.1:p.Gly246= | |
| XM_011531549.2:c.738C>T | XP_011529851.1:p.Gly246= | |
| XM_017007659.1:c.738C>T | XP_016863148.1:p.Gly246= | |
| NM_001286734.2:c.738C>T | NP_001273663.1:p.Gly246= | |
| NM_001813.3:c.738C>T MANE Select | NP_001804.2:p.Gly246= |