Canonical Allele Identifier: CA4965637
Gene: KCNV2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027206
ClinVar RCV Id: RCV001327769
dbSNP Id: rs149605734
ExAC: 9:2718561 G / A
gnomAD v2: 9-2718561-G-A
gnomAD v3: 9-2718561-G-A
gnomAD v4: 9-2718561-G-A
MyVariant Identifiers: chr9:g.2718561G>A (hg19) chr9:g.2718561G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718561G>A , CM000671.2:g.2718561G>A GRCh38
NC_000009.11:g.2718561G>A , CM000671.1:g.2718561G>A GRCh37
NC_000009.10:g.2708561G>A NCBI36
NG_012181.1:g.6036G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.822G>A MANE Select ENSP00000371514.3:p.Val274=
ENST00000382082.3:c.822G>A ENSP00000371514.3:p.Val274=
NM_133497.3:c.822G>A NP_598004.1:p.Val274=
XR_929202.1:n.1323G>A
XR_929203.1:n.1323G>A
NM_133497.4:c.822G>A MANE Select NP_598004.1:p.Val274=
Search 100 bp 5'
Search 100 bp 3'