Canonical Allele Identifier: CA2786054000
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576954G>T , CM000671.2:g.129576954G>T GRCh38
NC_000009.11:g.132339233G>T , CM000671.1:g.132339233G>T GRCh37
NC_000009.10:g.131379054G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1356G>T