Canonical Allele Identifier: CA2720468110
Gene:

Linked Data

dbSNP Id: rs985452516

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576705C>T , CM000671.2:g.129576705C>T GRCh38
NC_000009.11:g.132338984C>T , CM000671.1:g.132338984C>T GRCh37
NC_000009.10:g.131378805C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1107C>T