Canonical Allele Identifier: CA648937444
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557876T>C , CM000666.2:g.62557876T>C GRCh38
NC_000004.11:g.63423594T>C , CM000666.1:g.63423594T>C GRCh37
NC_000004.10:g.63106189T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5968T>C