Canonical Allele Identifier: CA2761911341
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558483T>C , CM000666.2:g.62558483T>C GRCh38
NC_000004.11:g.63424201T>C , CM000666.1:g.63424201T>C GRCh37
NC_000004.10:g.63106796T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5361T>C