Canonical Allele Identifier: CA890857274
Gene:

Linked Data

dbSNP Id: rs1172940780

Genomic Alleles

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

Transcript Alleles

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