Canonical Allele Identifier: CA1841175459
Gene:

Linked Data

dbSNP Id: rs1819674130

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551222G>C , CM000671.2:g.25551222G>C GRCh38
NC_000009.11:g.25551220G>C , CM000671.1:g.25551220G>C GRCh37
NC_000009.10:g.25541220G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-650C>G
XR_929525.2:n.674-650C>G