Linked Data
ClinVar Variation Id:
334242
dbSNP Id:
rs202141656
ExAC:
2:215845240 G / A
gnomAD v2:
2-215845240-G-A
gnomAD v3:
2-214980516-G-A
gnomAD v4:
2-214980516-G-A
COSMIC:
COSM1243873
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214980516G>A , CM000664.2:g.214980516G>A | GRCh38 |
| NC_000002.11:g.215845240G>A , CM000664.1:g.215845240G>A | GRCh37 |
| NC_000002.10:g.215553485G>A | NCBI36 |
| NG_007074.1:g.162912C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000272895.12:c.4707C>T MANE Select | ENSP00000272895.7:p.Gly1569= | |
| ENST00000272895.11:c.4707C>T | ENSP00000272895.7:p.Gly1569= | |
| ENST00000389661.4:c.3753C>T | ENSP00000374312.4:p.Gly1251= | |
| NM_015657.3:c.3753C>T | NP_056472.2:p.Gly1251= | |
| NM_173076.2:c.4707C>T | NP_775099.2:p.Gly1569= | |
| NR_103740.1:n.5007C>T | ||
| XM_011510951.1:c.4716C>T | XP_011509253.1:p.Gly1572= | |
| XM_011510952.1:c.4716C>T | XP_011509254.1:p.Gly1572= | |
| XM_011510951.2:c.4716C>T | XP_011509253.1:p.Gly1572= | |
| NM_173076.3:c.4707C>T MANE Select | NP_775099.2:p.Gly1569= | |
| NR_103740.2:n.5205C>T | ||
| NM_015657.4:c.3753C>T | NP_056472.2:p.Gly1251= |