Canonical Allele Identifier: CA2566619825
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661008G>T , CM000667.2:g.113661008G>T GRCh38
NC_000005.9:g.112996705G>T , CM000667.1:g.112996705G>T GRCh37
NC_000005.8:g.113024604G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27644G>T