Canonical Allele Identifier: CA4965619
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718517A>G , CM000671.2:g.2718517A>G GRCh38
NC_000009.11:g.2718517A>G , CM000671.1:g.2718517A>G GRCh37
NC_000009.10:g.2708517A>G NCBI36
NG_012181.1:g.5992A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.778A>G MANE Select ENSP00000371514.3:p.Lys260Glu
ENST00000382082.3:c.778A>G ENSP00000371514.3:p.Lys260Glu
NM_133497.3:c.778A>G NP_598004.1:p.Lys260Glu
XR_929202.1:n.1279A>G
XR_929203.1:n.1279A>G
NM_133497.4:c.778A>G MANE Select NP_598004.1:p.Lys260Glu