Canonical Allele Identifier: CA1841175442
Gene:

Linked Data

dbSNP Id: rs1819673774

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551188A>T , CM000671.2:g.25551188A>T GRCh38
NC_000009.11:g.25551186A>T , CM000671.1:g.25551186A>T GRCh37
NC_000009.10:g.25541186A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-616T>A
XR_929525.2:n.674-616T>A