Canonical Allele Identifier: CA2246165825
Gene:

Linked Data

dbSNP Id: rs1981891455

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137453A>C , CM000679.2:g.8137453A>C GRCh38
NC_000017.10:g.8040771A>C , CM000679.1:g.8040771A>C GRCh37
NC_000017.9:g.7981496A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1396A>C
XR_934203.1:n.70-2024A>C
XR_934202.2:n.414-1396A>C