Canonical Allele Identifier: CA2293960169
Gene:

Linked Data

dbSNP Id: rs2031433475

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756731T>G , CM000680.2:g.31756731T>G GRCh38
NC_000018.9:g.29336694T>G , CM000680.1:g.29336694T>G GRCh37
NC_000018.8:g.27590692T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5408T>G