Canonical Allele Identifier: CA16210586
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.170056852C>T , CM000666.2:g.170056852C>T GRCh38
NC_000004.11:g.170978003C>T , CM000666.1:g.170978003C>T GRCh37
NC_000004.10:g.171214578C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939440.1:n.180C>T