Canonical Allele Identifier: CA2714349790
Gene:

Linked Data

dbSNP Id: rs2128587764

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911532C>A , CM000669.2:g.30911532C>A GRCh38
NC_000007.13:g.30951147C>A , CM000669.1:g.30951147C>A GRCh37
NC_000007.12:g.30917672C>A NCBI36
NG_007475.2:g.63139C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-461C>A