Canonical Allele Identifier: CA1205766015
Gene:

Linked Data

dbSNP Id: rs1172940780

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649426G>T , CM000663.2:g.168649426G>T GRCh38
NC_000001.10:g.168618664G>T , CM000663.1:g.168618664G>T GRCh37
NC_000001.9:g.166885288G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8151C>A
XR_922259.2:n.332-8151C>A