Canonical Allele Identifier: CA2522309807
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.10667338A>T , CM000669.2:g.10667338A>T GRCh38
NC_000007.13:g.10706965A>T , CM000669.1:g.10706965A>T GRCh37
NC_000007.12:g.10673490A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147499.1:n.64-105761T>A
XR_001745090.1:n.376-7958A>T