Canonical Allele Identifier: CA1573933682
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660975C= , CM000667.2:g.113660975C= GRCh38
NC_000005.9:g.112996672C= , CM000667.1:g.112996672C= GRCh37
NC_000005.8:g.113024571C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27611C=