Canonical Allele Identifier: CA1222435240
Gene:

Linked Data

dbSNP Id: rs1659289557

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491639C>G , CM000663.2:g.220491639C>G GRCh38
NC_000001.10:g.220664981C>G , CM000663.1:g.220664981C>G GRCh37
NC_000001.9:g.218731604C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-595C>G
XR_001737822.1:n.557-595C>G