Canonical Allele Identifier: CA2762807096
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474175A>C , CM000666.2:g.99474175A>C GRCh38
NC_000004.11:g.100395332A>C , CM000666.1:g.100395332A>C GRCh37
NC_000004.10:g.100614355A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506494.1:n.243-2313T>G