Canonical Allele Identifier: CA1247519075
Gene:

Linked Data

dbSNP Id: rs1263053873

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534595C>A , CM000664.2:g.41534595C>A GRCh38
NC_000002.11:g.41761735C>A , CM000664.1:g.41761735C>A GRCh37
NC_000002.10:g.41615239C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3131G>T
XR_939997.1:n.146+3131G>T
XR_939997.2:n.9529+3131G>T