Canonical Allele Identifier: CA1573933639
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660886T= , CM000667.2:g.113660886T= GRCh38
NC_000005.9:g.112996583T= , CM000667.1:g.112996583T= GRCh37
NC_000005.8:g.113024482T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27522T=