Canonical Allele Identifier: CA1841175626
Gene:

Linked Data

dbSNP Id: rs1819678080

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551499A>T , CM000671.2:g.25551499A>T GRCh38
NC_000009.11:g.25551497A>T , CM000671.1:g.25551497A>T GRCh37
NC_000009.10:g.25541497A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-927T>A
XR_929525.2:n.674-927T>A