Canonical Allele Identifier: CA1697903981
Gene:

Linked Data

dbSNP Id: rs1791160720

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911543G>A , CM000669.2:g.30911543G>A GRCh38
NC_000007.13:g.30951158G>A , CM000669.1:g.30951158G>A GRCh37
NC_000007.12:g.30917683G>A NCBI36
NG_007475.2:g.63150G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-450G>A