Canonical Allele Identifier: CA2748988089
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458224A>T , CM000664.2:g.16458224A>T GRCh38
NC_000002.11:g.16639492A>T , CM000664.1:g.16639492A>T GRCh37
NC_000002.10:g.16502973A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3130T>A