Canonical Allele Identifier: CA1573933692
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661005A= , CM000667.2:g.113661005A= GRCh38
NC_000005.9:g.112996702A= , CM000667.1:g.112996702A= GRCh37
NC_000005.8:g.113024601A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27641A=