Linked Data
dbSNP Id:
rs771307273
ExAC:
12:7945730 T / C
gnomAD v2:
12-7945730-T-C
gnomAD v3:
12-7793134-T-C
gnomAD v4:
12-7793134-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.7793134T>C , CM000674.2:g.7793134T>C | GRCh38 |
| NC_000012.11:g.7945730T>C , CM000674.1:g.7945730T>C | GRCh37 |
| NC_000012.10:g.7836997T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229307.9:c.336T>C MANE Select | ENSP00000229307.4:p.Asp112= | |
| ENST00000229307.8:c.336T>C | ENSP00000229307.4:p.Asp112= | |
| ENST00000526286.1:c.336T>C | ENSP00000435288.1:p.Asp112= | |
| ENST00000526434.2:n.480T>C | ||
| ENST00000541267.5:c.264T>C | ENSP00000444434.1:p.Asp88= | |
| NM_001297698.1:c.336T>C | NP_001284627.1:p.Asp112= | |
| NM_024865.3:c.336T>C | NP_079141.2:p.Asp112= | |
| XM_011520850.1:c.336T>C | XP_011519152.1:p.Asp112= | |
| XM_011520851.1:c.264T>C | XP_011519153.1:p.Asp88= | |
| XM_011520852.1:c.-37T>C | XP_011519154.1:n.-37T>C | |
| NM_024865.4:c.336T>C MANE Select | NP_079141.2:p.Asp112= | |
| NM_001297698.2:c.336T>C | NP_001284627.1:p.Asp112= |