Linked Data
ClinVar Variation Id:
289246
dbSNP Id:
rs886044132
gnomAD v2:
5-156016303-T-C
gnomAD v4:
5-156589293-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.156589293T>C , CM000667.2:g.156589293T>C | GRCh38 |
| NC_000005.9:g.156016303T>C , CM000667.1:g.156016303T>C | GRCh37 |
| NC_000005.8:g.155948881T>C | NCBI36 |
| NG_008693.2:g.723950T>C , LRG_205:g.723950T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337851.9:c.357T>C MANE Select | ENSP00000338343.4:p.Thr119= | |
| ENST00000337851.8:c.357T>C | ENSP00000338343.4:p.Thr119= | |
| ENST00000435422.7:c.354T>C | ENSP00000403003.2:p.Thr118= | |
| ENST00000517913.5:c.357T>C | ENSP00000429378.1:p.Thr119= | |
| NM_000337.5:c.357T>C , LRG_205t1:c.357T>C | NP_000328.2:p.Thr119= | |
| NM_001128209.1:c.354T>C | NP_001121681.1:p.Thr118= | |
| NM_172244.2:c.357T>C | NP_758447.1:p.Thr119= | |
| XM_005265966.3:c.357T>C | XP_005266023.1:p.Thr119= | |
| XM_005265967.1:c.357T>C | XP_005266024.1:p.Thr119= | |
| XM_006714911.2:c.357T>C | XP_006714974.1:p.Thr119= | |
| XM_011534621.1:c.354T>C | XP_011532923.1:p.Thr118= | |
| XM_005265966.5:c.357T>C | XP_005266023.1:p.Thr119= | |
| XM_005265967.2:c.357T>C | XP_005266024.1:p.Thr119= | |
| XM_011534621.2:c.354T>C | XP_011532923.1:p.Thr118= | |
| XM_017009723.2:c.357T>C | XP_016865212.1:p.Thr119= | |
| XM_017009724.1:c.357T>C | XP_016865213.1:p.Thr119= | |
| NM_001128209.2:c.354T>C | NP_001121681.1:p.Thr118= | |
| NM_172244.3:c.357T>C | NP_758447.1:p.Thr119= | |
| NM_000337.6:c.357T>C MANE Select | NP_000328.2:p.Thr119= |