Canonical Allele Identifier: CA2718875007
Gene:

Linked Data

dbSNP Id: rs1478364690

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551204C>T , CM000671.2:g.25551204C>T GRCh38
NC_000009.11:g.25551202C>T , CM000671.1:g.25551202C>T GRCh37
NC_000009.10:g.25541202C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-632G>A
XR_929525.2:n.674-632G>A