Canonical Allele Identifier: CA1284674307
Gene:

Linked Data

dbSNP Id: rs1680376090

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884143G>A , CM000664.2:g.122884143G>A GRCh38
NC_000002.11:g.123641719G>A , CM000664.1:g.123641719G>A GRCh37
NC_000002.10:g.123358189G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-799G>A
XR_001739692.1:n.1451-799G>A
XR_923292.2:n.1358-799G>A