Canonical Allele Identifier: CA787553439
Gene:

Linked Data

dbSNP Id: rs1192705819

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601527A>G , CM000666.2:g.134601527A>G GRCh38
NC_000004.11:g.135522682A>G , CM000666.1:g.135522682A>G GRCh37
NC_000004.10:g.135742132A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14168A>G
XR_939214.1:n.392+14168A>G
XR_939214.2:n.392+14168A>G