Canonical Allele Identifier: CA2284269287
Gene:

Linked Data

dbSNP Id: rs1418885717

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382829A>G , CM000680.2:g.10382829A>G GRCh38
NC_000018.9:g.10382826A>G , CM000680.1:g.10382826A>G GRCh37
NC_000018.8:g.10372826A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1476A>G