Linked Data
gnomAD v4:
19-5903813-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.5903813T>C , CM000681.2:g.5903813T>C | GRCh38 |
| NC_000019.9:g.5903824T>C , CM000681.1:g.5903824T>C | GRCh37 |
| NC_000019.8:g.5854824T>C | NCBI36 |
| NG_027808.1:g.5201A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000591160.1:n.194A>G | ||
| NM_001193375.1:c.-105A>G | NP_001180304.1:n.-105A>G | |
| NM_175614.4:c.-105A>G | NP_783313.1:n.-105A>G | |
| NR_034166.2:n.201A>G |