Canonical Allele Identifier: CA861674135
Gene:

Linked Data

dbSNP Id: rs1438858756

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787618A>T , CM000671.2:g.1787618A>T GRCh38
NC_000009.11:g.1787618A>T , CM000671.1:g.1787618A>T GRCh37
NC_000009.10:g.1777618A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746599.1:n.142+68706A>T