Canonical Allele Identifier: CA1841175395
Gene:

Linked Data

dbSNP Id: rs1819672377

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551099A>G , CM000671.2:g.25551099A>G GRCh38
NC_000009.11:g.25551097A>G , CM000671.1:g.25551097A>G GRCh37
NC_000009.10:g.25541097A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-527T>C
XR_929525.2:n.674-527T>C