Canonical Allele Identifier: CA672772713
Gene:

Linked Data

dbSNP Id: rs11219068

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123204711G>T , CM000673.2:g.123204711G>T GRCh38
NC_000011.9:g.123075419G>T , CM000673.1:g.123075419G>T GRCh37
NC_000011.8:g.122580629G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948116.1:n.250+150G>T
XR_948117.1:n.250+150G>T
XR_948116.2:n.524+150G>T