Linked Data
gnomAD v4:
19-12887191-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887191T>A , CM000681.2:g.12887191T>A | GRCh38 |
| NC_000019.9:g.12998005T>A , CM000681.1:g.12998005T>A | GRCh37 |
| NC_000019.8:g.12859005T>A | NCBI36 |
| NG_009292.1:g.1032T>A | |
| NG_013087.1:g.5013A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.-51A>T MANE Select | ENSP00000264834.3:n.-51A>T | |
| NM_006563.3:c.-51A>T | NP_006554.1:n.-51A>T | |
| NM_006563.4:c.-51A>T | NP_006554.1:n.-51A>T | |
| NM_006563.5:c.-51A>T MANE Select | NP_006554.1:n.-51A>T |