Canonical Allele Identifier: CA2776834906
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87913777C>T , CM000669.2:g.87913777C>T GRCh38
NC_000007.13:g.87543092C>T , CM000669.1:g.87543092C>T GRCh37
NC_000007.12:g.87381028C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927723.1:n.148+124G>A
XR_927724.1:n.192+124G>A