Canonical Allele Identifier: CA1202763093
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161493811G>C , CM000663.2:g.161493811G>C GRCh38
NC_000001.10:g.161463601G>C , CM000663.1:g.161463601G>C GRCh37
NC_000001.9:g.159730225G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922214.1:n.2011+192G>C
XR_922214.2:n.2960+192G>C