Canonical Allele Identifier: CA2762807097
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474219A>G , CM000666.2:g.99474219A>G GRCh38
NC_000004.11:g.100395376A>G , CM000666.1:g.100395376A>G GRCh37
NC_000004.10:g.100614399A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506494.1:n.243-2357T>C