Linked Data
dbSNP Id:
rs999481918
gnomAD v4:
15-58749922-C-T
MyVariant Identifiers:
chr15:g.58749922C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.58749922C>T , CM000677.2:g.58749922C>T | GRCh38 |
| NC_000015.9:g.59042121C>T , CM000677.1:g.59042121C>T | GRCh37 |
| NC_000015.8:g.56829413C>T | NCBI36 |
| NG_033876.1:g.5057G>A | |
| NG_033876.2:g.4786G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260408.7:c.-388G>A | ENSP00000260408.3:n.-388G>A | |
| NM_001110.3:c.-388G>A | NP_001101.1:n.-388G>A | |
| NM_001320570.1:c.-388G>A | NP_001307499.1:n.-388G>A |