Linked Data
gnomAD v4:
3-81648975-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81648975G>A , CM000665.2:g.81648975G>A | GRCh38 |
| NC_000003.11:g.81698126G>A , CM000665.1:g.81698126G>A | GRCh37 |
| NC_000003.10:g.81780816G>A | NCBI36 |
| NG_011810.1:g.117826C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.572C>T MANE Select | ENSP00000410833.2:p.Pro191Leu | |
| ENST00000429644.6:c.572C>T | ENSP00000410833.2:p.Pro191Leu | |
| ENST00000486920.1:n.568C>T | ||
| ENST00000489715.1:c.449C>T | ENSP00000419638.1:p.Pro150Leu | |
| ENST00000498468.1:n.100C>T | ||
| NM_000158.3:c.572C>T | NP_000149.3:p.Pro191Leu | |
| NM_000158.4:c.572C>T MANE Select | NP_000149.4:p.Pro191Leu |