Canonical Allele Identifier: CA30669376
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153023685G>C , CM000663.2:g.153023685G>C GRCh38
NC_000001.10:g.152996161G>C , CM000663.1:g.152996161G>C GRCh37
NC_000001.9:g.151262785G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922151.1:n.101-258G>C
XR_922152.1:n.191-258G>C