Canonical Allele Identifier: CA463853634
Gene: KCNV2 HGNC NCBI

Linked Data

gnomAD v4: 9-2718564-G-A
MyVariant Identifiers: chr9:g.2718564G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718564G>A , CM000671.2:g.2718564G>A GRCh38
NC_000009.11:g.2718564G>A , CM000671.1:g.2718564G>A GRCh37
NC_000009.10:g.2708564G>A NCBI36
NG_012181.1:g.6039G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.825G>A MANE Select ENSP00000371514.3:p.Val275=
ENST00000382082.3:c.825G>A ENSP00000371514.3:p.Val275=
NM_133497.3:c.825G>A NP_598004.1:p.Val275=
XR_929202.1:n.1326G>A
XR_929203.1:n.1326G>A
NM_133497.4:c.825G>A MANE Select NP_598004.1:p.Val275=