Canonical Allele Identifier: CA1800733855
Gene:

Linked Data

dbSNP Id: rs1810441855

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535718C>G , CM000670.2:g.88535718C>G GRCh38
NC_000008.10:g.89547947C>G , CM000670.1:g.89547947C>G GRCh37
NC_000008.9:g.89617063C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10799G>C
XR_001745653.2:n.286-6962C>G
XR_928383.3:n.1475+10799G>C