Canonical Allele Identifier: CA1635885278
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.68627895A>T , CM000668.2:g.68627895A>T GRCh38
NC_000006.11:g.69337787A>T , CM000668.1:g.69337787A>T GRCh37
NC_000006.10:g.69394508A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942664.1:n.1978T>A