Canonical Allele Identifier: CA987758068
Gene:

Linked Data

dbSNP Id: rs1969409527

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382927T>G , CM000680.2:g.10382927T>G GRCh38
NC_000018.9:g.10382924T>G , CM000680.1:g.10382924T>G GRCh37
NC_000018.8:g.10372924T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1574T>G