Canonical Allele Identifier: CA151622548
Gene:

Linked Data

dbSNP Id: rs537277117

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765649G>A , CM000668.2:g.163765649G>A GRCh38
NC_000006.11:g.164186681G>A , CM000668.1:g.164186681G>A GRCh37
NC_000006.10:g.164106671G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6220G>A
XR_001744454.1:n.369+6261G>A
XR_001744455.1:n.346+6284G>A