Canonical Allele Identifier: CA2263926978
Gene:

Linked Data

dbSNP Id: rs1908570845

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211849T>G , CM000679.2:g.50211849T>G GRCh38
NC_000017.10:g.48289210T>G , CM000679.1:g.48289210T>G GRCh37
NC_000017.9:g.45644209T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-1986T>G