Canonical Allele Identifier: CA300391540
Gene:

Linked Data

dbSNP Id: rs938790887

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645814A>G , CM000680.2:g.49645814A>G GRCh38
NC_000018.9:g.47172184A>G , CM000680.1:g.47172184A>G GRCh37
NC_000018.8:g.45426182A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16220A>G
XR_001753446.1:n.898-16220A>G