Canonical Allele Identifier: CA1573933699
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661032T= , CM000667.2:g.113661032T= GRCh38
NC_000005.9:g.112996729T= , CM000667.1:g.112996729T= GRCh37
NC_000005.8:g.113024628T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27668T=