Canonical Allele Identifier: CA1889304374
Gene:

Linked Data

dbSNP Id: rs1833394665

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8659170A>T , CM000672.2:g.8659170A>T GRCh38
NC_000010.10:g.8701133A>T , CM000672.1:g.8701133A>T GRCh37
NC_000010.9:g.8741139A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.178T>A
XR_001747277.1:n.147T>A