Canonical Allele Identifier: CA2246165720
Gene:

Linked Data

dbSNP Id: rs1244551374

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137361C>T , CM000679.2:g.8137361C>T GRCh38
NC_000017.10:g.8040679C>T , CM000679.1:g.8040679C>T GRCh37
NC_000017.9:g.7981404C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1488C>T
XR_934203.1:n.70-2116C>T
XR_934202.2:n.414-1488C>T