Canonical Allele Identifier: CA1841175600
Gene:

Linked Data

dbSNP Id: rs1819677360

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551454T>G , CM000671.2:g.25551454T>G GRCh38
NC_000009.11:g.25551452T>G , CM000671.1:g.25551452T>G GRCh37
NC_000009.10:g.25541452T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-882A>C
XR_929525.2:n.674-882A>C