Canonical Allele Identifier: CA1328655609
Gene:

Linked Data

dbSNP Id: rs1689247550

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216617G>A , CM000664.2:g.218216617G>A GRCh38
NC_000002.11:g.219081340G>A , CM000664.1:g.219081340G>A GRCh37
NC_000002.10:g.218789585G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241416.2:n.328C>T
XR_923908.1:n.325C>T