Linked Data
gnomAD v4:
19-40285422-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40285422C>T , CM000681.2:g.40285422C>T | GRCh38 |
| NC_000019.9:g.40791329C>T , CM000681.1:g.40791329C>T | GRCh37 |
| NC_000019.8:g.45483169C>T | NCBI36 |
| NG_012038.2:g.4937G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000578123.5:c.-85+26G>A | ENSP00000462022.1:n.-85+26G>A | |
| XM_011526620.1:c.-85+26G>A | XP_011524922.1:n.-85+26G>A |