Canonical Allele Identifier: CA298296852
Gene:

Linked Data

dbSNP Id: rs10502575

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756628A>G , CM000680.2:g.31756628A>G GRCh38
NC_000018.9:g.29336591A>G , CM000680.1:g.29336591A>G GRCh37
NC_000018.8:g.27590589A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5511A>G