Linked Data
dbSNP Id:
rs1394104178
gnomAD v4:
9-35657974-G-T
MyVariant Identifiers:
chr9:g.35657971G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35657974G>T , CM000671.2:g.35657974G>T | GRCh38 |
| NC_000009.11:g.35657971G>T , CM000671.1:g.35657971G>T | GRCh37 |
| NC_000009.10:g.35647971G>T | NCBI36 |
| NG_017041.1:g.5045C>A , LRG_163:g.5045C>A | |
| NG_033120.1:g.4685G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003051.3:n.45C>A , LRG_163t1:n.45C>A |