Canonical Allele Identifier: CA1841175397
Gene:

Linked Data

dbSNP Id: rs1332158

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551100A>C , CM000671.2:g.25551100A>C GRCh38
NC_000009.11:g.25551098A>C , CM000671.1:g.25551098A>C GRCh37
NC_000009.10:g.25541098A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-528T>G
XR_929525.2:n.674-528T>G