Linked Data
gnomAD v4:
19-5903815-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.5903815G>C , CM000681.2:g.5903815G>C | GRCh38 |
| NC_000019.9:g.5903826G>C , CM000681.1:g.5903826G>C | GRCh37 |
| NC_000019.8:g.5854826G>C | NCBI36 |
| NG_027808.1:g.5199C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000591160.1:n.192C>G | ||
| NM_001193375.1:c.-107C>G | NP_001180304.1:n.-107C>G | |
| NM_175614.4:c.-107C>G | NP_783313.1:n.-107C>G | |
| NR_034166.2:n.199C>G |