Canonical Allele Identifier: CA2523617018
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458164G>T , CM000664.2:g.16458164G>T GRCh38
NC_000002.11:g.16639432G>T , CM000664.1:g.16639432G>T GRCh37
NC_000002.10:g.16502913G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3070C>A