Canonical Allele Identifier: CA1828289311
Gene: KCNV2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.824T= MANE Select ENSP00000371514.3:p.Val275=
ENST00000382082.3:c.824T= ENSP00000371514.3:p.Val275=
NM_133497.3:c.824T= NP_598004.1:p.Val275=
XR_929202.1:n.1325T=
XR_929203.1:n.1325T=
NM_133497.4:c.824T= MANE Select NP_598004.1:p.Val275=