Canonical Allele Identifier: CA1318169526
Gene:

Linked Data

dbSNP Id: rs1688124325

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007201A>G , CM000664.2:g.195007201A>G GRCh38
NC_000002.11:g.195871925A>G , CM000664.1:g.195871925A>G GRCh37
NC_000002.10:g.195580170A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52234T>C