Linked Data
gnomAD v4:
19-40285476-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40285476C>T , CM000681.2:g.40285476C>T | GRCh38 |
| NC_000019.9:g.40791383C>T , CM000681.1:g.40791383C>T | GRCh37 |
| NC_000019.8:g.45483223C>T | NCBI36 |
| NG_012038.2:g.4883G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000578123.5:c.-113G>A | ENSP00000462022.1:n.-113G>A | |
| XM_011526620.1:c.-113G>A | XP_011524922.1:n.-113G>A |