Canonical Allele Identifier: CA1150659665
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.4608610G>C , CM000663.2:g.4608610G>C GRCh38
NC_000001.10:g.4668670G>C , CM000663.1:g.4668670G>C GRCh37
NC_000001.9:g.4568530G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001737775.1:n.489+567G>C