Canonical Allele Identifier: CA372796080
Gene: KCNV2 HGNC NCBI

Linked Data

gnomAD v4: 9-2717969-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717969A>T , CM000671.2:g.2717969A>T GRCh38
NC_000009.11:g.2717969A>T , CM000671.1:g.2717969A>T GRCh37
NC_000009.10:g.2707969A>T NCBI36
NG_012181.1:g.5444A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.230A>T MANE Select ENSP00000371514.3:p.Gln77Leu
ENST00000382082.3:c.230A>T ENSP00000371514.3:p.Gln77Leu
NM_133497.3:c.230A>T NP_598004.1:p.Gln77Leu
XR_929202.1:n.731A>T
XR_929203.1:n.731A>T
NM_133497.4:c.230A>T MANE Select NP_598004.1:p.Gln77Leu