Canonical Allele Identifier: CA372799550
Gene: KCNV2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718559G>T , CM000671.2:g.2718559G>T GRCh38
NC_000009.11:g.2718559G>T , CM000671.1:g.2718559G>T GRCh37
NC_000009.10:g.2708559G>T NCBI36
NG_012181.1:g.6034G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.820G>T MANE Select ENSP00000371514.3:p.Val274Leu
ENST00000382082.3:c.820G>T ENSP00000371514.3:p.Val274Leu
NM_133497.3:c.820G>T NP_598004.1:p.Val274Leu
XR_929202.1:n.1321G>T
XR_929203.1:n.1321G>T
NM_133497.4:c.820G>T MANE Select NP_598004.1:p.Val274Leu