Canonical Allele Identifier: CA1905919973
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318546C= , CM000672.2:g.43318546C= GRCh38
NC_000010.10:g.43813994C= , CM000672.1:g.43813994C= GRCh37
NC_000010.9:g.43134000C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.59C=
XR_945902.2:n.149C=