Canonical Allele Identifier: CA1318169532
Gene:

Linked Data

dbSNP Id: rs1688124593

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007218T>G , CM000664.2:g.195007218T>G GRCh38
NC_000002.11:g.195871942T>G , CM000664.1:g.195871942T>G GRCh37
NC_000002.10:g.195580187T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52217A>C