Canonical Allele Identifier:
CA14382128
Gene:
Linked Data
dbSNP Id:
rs17760296
gnomAD v2:
17-54615617-T-G
gnomAD v3:
17-56538256-T-G
gnomAD v4:
17-56538256-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56538256T>G , CM000679.2:g.56538256T>G | GRCh38 |
| NC_000017.10:g.54615617T>G , CM000679.1:g.54615617T>G | GRCh37 |
| NC_000017.9:g.51970616T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_934871.1:n.245-422A>C | ||
| XR_934872.1:n.245-422A>C | ||
| XR_002958121.1:n.245-422A>C |