Canonical Allele Identifier: CA1899263454
Gene:

Linked Data

dbSNP Id: rs1839589155

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201650T>G , CM000672.2:g.30201650T>G GRCh38
NC_000010.10:g.30490579T>G , CM000672.1:g.30490579T>G GRCh37
NC_000010.9:g.30530585T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930791.1:n.1193-1837T>G
XR_930791.2:n.1449-1837T>G