Linked Data
dbSNP Id:
rs937409631
gnomAD v2:
1-11107015-C-T
gnomAD v3:
1-11046958-C-T
gnomAD v4:
1-11046958-C-T
COSMIC:
COSM893694
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11046958C>T , CM000663.2:g.11046958C>T | GRCh38 |
| NC_000001.10:g.11107015C>T , CM000663.1:g.11107015C>T | GRCh37 |
| NC_000001.9:g.11029602C>T | NCBI36 |
| NG_007289.1:g.5271G>A | |
| NG_007289.2:g.5271G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699958.1:c.167G>A | ENSP00000514717.1:p.Arg56His | |
| ENST00000700088.1:c.167G>A | ENSP00000514787.1:p.Arg56His | |
| ENST00000700089.1:c.167G>A | ENSP00000514788.1:p.Arg56His | |
| ENST00000700090.1:c.167G>A | ENSP00000514789.1:p.Arg56His | |
| ENST00000700091.1:c.167G>A | ENSP00000514790.1:p.Arg56His | |
| ENST00000700092.1:c.167G>A | ENSP00000514791.1:p.Arg56His | |
| ENST00000700093.1:c.167G>A | ENSP00000514792.1:p.Arg56His | |
| ENST00000700094.1:c.167G>A | ENSP00000514793.1:p.Arg56His | |
| ENST00000700095.1:c.167G>A | ENSP00000514794.1:p.Arg56His | |
| ENST00000700096.1:c.167G>A | ENSP00000514795.1:p.Arg56His | |
| ENST00000700097.1:c.167G>A | ENSP00000514796.1:p.Arg56His | |
| ENST00000400897.8:c.167G>A MANE Select | ENSP00000383690.3:p.Arg56His | |
| ENST00000400897.7:c.167G>A | ENSP00000383690.3:p.Arg56His | |
| ENST00000400898.3:c.167G>A | ENSP00000383691.3:p.Arg56His | |
| ENST00000480221.1:n.187G>A | ||
| NM_006610.3:c.167G>A | NP_006601.2:p.Arg56His | |
| NM_139208.2:c.167G>A | NP_631947.1:p.Arg56His | |
| XM_017000097.1:c.167G>A | XP_016855586.1:p.Arg56His | |
| XR_001736931.1:n.199G>A | ||
| XR_001736932.1:n.199G>A | ||
| XR_002958895.1:n.199G>A | ||
| NM_006610.4:c.167G>A MANE Select | NP_006601.2:p.Arg56His | |
| NM_139208.3:c.167G>A | NP_631947.1:p.Arg56His |