Canonical Allele Identifier: CA2284269327
Gene:

Linked Data

dbSNP Id: rs1969409129

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382905G>T , CM000680.2:g.10382905G>T GRCh38
NC_000018.9:g.10382902G>T , CM000680.1:g.10382902G>T GRCh37
NC_000018.8:g.10372902G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1552G>T