Canonical Allele Identifier: CA821943335
Gene:

Linked Data

dbSNP Id: rs1265250438

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765597A>G , CM000668.2:g.163765597A>G GRCh38
NC_000006.11:g.164186629A>G , CM000668.1:g.164186629A>G GRCh37
NC_000006.10:g.164106619A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6168A>G
XR_001744454.1:n.369+6209A>G
XR_001744455.1:n.346+6232A>G