Canonical Allele Identifier: CA11326762
Gene:

Linked Data

dbSNP Id: rs12619285

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.212959321A>G , CM000664.2:g.212959321A>G GRCh38
NC_000002.11:g.213824045A>G , CM000664.1:g.213824045A>G GRCh37
NC_000002.10:g.213532290A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923849.1:n.484+6063T>C
XR_001739869.1:n.2124+6063T>C