Canonical Allele Identifier: CA1841175559
Gene:

Linked Data

dbSNP Id: rs1819676464

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551398T>C , CM000671.2:g.25551398T>C GRCh38
NC_000009.11:g.25551396T>C , CM000671.1:g.25551396T>C GRCh37
NC_000009.10:g.25541396T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-826A>G
XR_929525.2:n.674-826A>G