Linked Data
gnomAD v4:
9-129814196-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129814196C>A , CM000671.2:g.129814196C>A | GRCh38 |
| NC_000009.11:g.132576475C>A , CM000671.1:g.132576475C>A | GRCh37 |
| NC_000009.10:g.131616296C>A | NCBI36 |
| NG_008049.1:g.14967G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.775G>T MANE Select | ENSP00000345719.4:p.Asp259Tyr | |
| ENST00000651202.1:c.*43G>T | ENSP00000498222.1:n.*43G>T | |
| ENST00000351698.4:c.775G>T | ENSP00000345719.4:p.Asp259Tyr | |
| ENST00000474192.1:n.359G>T | ||
| NM_000113.2:c.775G>T | NP_000104.1:p.Asp259Tyr | |
| XR_929731.1:n.1102G>T | ||
| XR_929731.3:n.970G>T | ||
| NM_000113.3:c.775G>T MANE Select | NP_000104.1:p.Asp259Tyr |