Canonical Allele Identifier: CA1886681894
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3375959C= , CM000672.2:g.3375959C= GRCh38
NC_000010.10:g.3418151C= , CM000672.1:g.3418151C= GRCh37
NC_000010.9:g.3408151C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+57103C=