Canonical Allele Identifier: CA10683559
Gene: KCNA3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1058184

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672850A>C , CM000663.2:g.110672850A>C GRCh38
NC_000001.10:g.111215472A>C , CM000663.1:g.111215472A>C GRCh37
NC_000001.9:g.111016995A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002232.4:c.*232T>G VV NP_002223.3:p.=
NR_109845.1:n.218+387T>G
XR_001738182.1:n.569-13524A>C
XR_001738183.1:n.567-13524A>C
XR_001738184.1:n.573-13524A>C
XR_001738185.1:n.568-13524A>C
XR_001738186.1:n.572-13524A>C
XR_001738187.1:n.570-13524A>C
NM_002232.5:c.*232T>G VV MANE Preferred
ENST00000369769.3:c.*232T>G ENSP00000358784.2:p.=