Canonical Allele Identifier: CA300391542
Gene:

Linked Data

dbSNP Id: rs1025800603

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645834A>T , CM000680.2:g.49645834A>T GRCh38
NC_000018.9:g.47172204A>T , CM000680.1:g.47172204A>T GRCh37
NC_000018.8:g.45426202A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16200A>T
XR_001753446.1:n.898-16200A>T