Canonical Allele Identifier: CA987758025
Gene:

Linked Data

dbSNP Id: rs1877487010

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382818A>G , CM000680.2:g.10382818A>G GRCh38
NC_000018.9:g.10382815A>G , CM000680.1:g.10382815A>G GRCh37
NC_000018.8:g.10372815A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1465A>G