Canonical Allele Identifier: CA1697903951
Gene:

Linked Data

dbSNP Id: rs1791160303

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911524G>A , CM000669.2:g.30911524G>A GRCh38
NC_000007.13:g.30951139G>A , CM000669.1:g.30951139G>A GRCh37
NC_000007.12:g.30917664G>A NCBI36
NG_007475.2:g.63131G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-469G>A