Linked Data
gnomAD v4:
6-131851238-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131851238G>A , CM000668.2:g.131851238G>A | GRCh38 |
| NC_000006.11:g.132172378G>A , CM000668.1:g.132172378G>A | GRCh37 |
| NC_000006.10:g.132214071G>A | NCBI36 |
| NG_008206.1:g.48223G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647893.1:c.527G>A MANE Select | ENSP00000498074.1:p.Cys176Tyr | |
| ENST00000650147.1:c.205G>A | ||
| ENST00000650437.1:c.108+1132G>A | ||
| ENST00000360971.6:c.527G>A | ENSP00000354238.2:p.Cys176Tyr | |
| ENST00000486853.1:n.547G>A | ||
| ENST00000513998.5:c.527G>A | ENSP00000422424.1:p.Cys176Tyr | |
| NM_006208.2:c.527G>A | NP_006199.2:p.Cys176Tyr | |
| NM_006208.3:c.527G>A MANE Select | NP_006199.2:p.Cys176Tyr |