Canonical Allele Identifier: CA372799565
Gene: KCNV2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718563T>G , CM000671.2:g.2718563T>G GRCh38
NC_000009.11:g.2718563T>G , CM000671.1:g.2718563T>G GRCh37
NC_000009.10:g.2708563T>G NCBI36
NG_012181.1:g.6038T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.824T>G MANE Select ENSP00000371514.3:p.Val275Gly
ENST00000382082.3:c.824T>G ENSP00000371514.3:p.Val275Gly
NM_133497.3:c.824T>G NP_598004.1:p.Val275Gly
XR_929202.1:n.1325T>G
XR_929203.1:n.1325T>G
NM_133497.4:c.824T>G MANE Select NP_598004.1:p.Val275Gly