Canonical Allele Identifier: CA1841175456
Gene:

Linked Data

dbSNP Id: rs1819674068

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551220A>C , CM000671.2:g.25551220A>C GRCh38
NC_000009.11:g.25551218A>C , CM000671.1:g.25551218A>C GRCh37
NC_000009.10:g.25541218A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-648T>G
XR_929525.2:n.674-648T>G