Canonical Allele Identifier: CA1139827905
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2581777C= , CM000663.2:g.2581777C= GRCh38
NC_000001.10:g.2513216C= , CM000663.1:g.2513216C= GRCh37
NC_000001.9:g.2503076C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121638.1:n.162+127C=