Canonical Allele Identifier: CA1816697715
Gene:

Linked Data

dbSNP Id: rs1586355429

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.123753497A>G , CM000670.2:g.123753497A>G GRCh38
NC_000008.10:g.124765737A>G , CM000670.1:g.124765737A>G GRCh37
NC_000008.9:g.124834918A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928607.1:n.153-11286A>G
XR_928607.3:n.324-11286A>G