Canonical Allele Identifier: CA1800733857
Gene:

Linked Data

dbSNP Id: rs1586113120

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535720G>C , CM000670.2:g.88535720G>C GRCh38
NC_000008.10:g.89547949G>C , CM000670.1:g.89547949G>C GRCh37
NC_000008.9:g.89617065G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10797C>G
XR_001745653.2:n.286-6960G>C
XR_928383.3:n.1475+10797C>G