Canonical Allele Identifier: CA1828289308
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718562G= , CM000671.2:g.2718562G= GRCh38
NC_000009.11:g.2718562G= , CM000671.1:g.2718562G= GRCh37
NC_000009.10:g.2708562G= NCBI36
NG_012181.1:g.6037G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.823G= MANE Select ENSP00000371514.3:p.Val275=
ENST00000382082.3:c.823G= ENSP00000371514.3:p.Val275=
NM_133497.3:c.823G= NP_598004.1:p.Val275=
XR_929202.1:n.1324G=
XR_929203.1:n.1324G=
NM_133497.4:c.823G= MANE Select NP_598004.1:p.Val275=