Canonical Allele Identifier: CA2302316769
Gene:

Linked Data

dbSNP Id: rs2021992732

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645821A>G , CM000680.2:g.49645821A>G GRCh38
NC_000018.9:g.47172191A>G , CM000680.1:g.47172191A>G GRCh37
NC_000018.8:g.45426189A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16213A>G
XR_001753446.1:n.898-16213A>G