Canonical Allele Identifier: CA4965639
Gene: KCNV2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026169
ClinVar RCV Id: RCV001326588
dbSNP Id: rs199923365
gnomAD v2: 9-2718566-C-T
gnomAD v3: 9-2718566-C-T
gnomAD v4: 9-2718566-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718566C>T , CM000671.2:g.2718566C>T GRCh38
NC_000009.11:g.2718566C>T , CM000671.1:g.2718566C>T GRCh37
NC_000009.10:g.2708566C>T NCBI36
NG_012181.1:g.6041C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.827C>T MANE Select ENSP00000371514.3:p.Ala276Val
ENST00000382082.3:c.827C>T ENSP00000371514.3:p.Ala276Val
NM_133497.3:c.827C>T NP_598004.1:p.Ala276Val
XR_929202.1:n.1328C>T
XR_929203.1:n.1328C>T
NM_133497.4:c.827C>T MANE Select NP_598004.1:p.Ala276Val