Canonical Allele Identifier: CA2013540863
Gene:

Linked Data

dbSNP Id: rs1864899114

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5284224C>T , CM000674.2:g.5284224C>T GRCh38
NC_000012.11:g.5393390C>T , CM000674.1:g.5393390C>T GRCh37
NC_000012.10:g.5263651C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931576.1:n.611+7335C>T
XR_931577.1:n.611+7335C>T
XR_001748970.1:n.594+7335C>T