Canonical Allele Identifier: CA10989572
Gene:

Linked Data

dbSNP Id: rs1320976

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169104108G>A , CM000663.2:g.169104108G>A GRCh38
NC_000001.10:g.169073346G>A , CM000663.1:g.169073346G>A GRCh37
NC_000001.9:g.167339970G>A NCBI36
NG_023230.1:g.2400G>A

Transcript Alleles

HGVS Amino-acid change
XM_011510287.1:c.-1188G>A XP_011508589.1:n.-1188G>A