Canonical Allele Identifier: CA372799555
Gene: KCNV2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718560T>C , CM000671.2:g.2718560T>C GRCh38
NC_000009.11:g.2718560T>C , CM000671.1:g.2718560T>C GRCh37
NC_000009.10:g.2708560T>C NCBI36
NG_012181.1:g.6035T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.821T>C MANE Select ENSP00000371514.3:p.Val274Ala
ENST00000382082.3:c.821T>C ENSP00000371514.3:p.Val274Ala
NM_133497.3:c.821T>C NP_598004.1:p.Val274Ala
XR_929202.1:n.1322T>C
XR_929203.1:n.1322T>C
NM_133497.4:c.821T>C MANE Select NP_598004.1:p.Val274Ala