Canonical Allele Identifier: CA1880834542
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576960C= , CM000671.2:g.129576960C= GRCh38
NC_000009.11:g.132339239C= , CM000671.1:g.132339239C= GRCh37
NC_000009.10:g.131379060C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1362C=