Canonical Allele Identifier: CA1349198988
Gene:

Linked Data

dbSNP Id: rs2095171364

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.18975809A>C , CM000665.2:g.18975809A>C GRCh38
NC_000003.11:g.19017301A>C , CM000665.1:g.19017301A>C GRCh37
NC_000003.10:g.18992305A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940638.1:n.437+7741T>G
XR_001740612.1:n.774+7741T>G
XR_001740613.1:n.303+9402A>C
XR_001740614.1:n.303+9402A>C
XR_001740615.1:n.304+9402A>C
XR_001740616.1:n.304+9402A>C