Canonical Allele Identifier: CA372795767
Gene: KCNV2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717869C>G , CM000671.2:g.2717869C>G GRCh38
NC_000009.11:g.2717869C>G , CM000671.1:g.2717869C>G GRCh37
NC_000009.10:g.2707869C>G NCBI36
NG_012181.1:g.5344C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.130C>G MANE Select ENSP00000371514.3:p.His44Asp
ENST00000382082.3:c.130C>G ENSP00000371514.3:p.His44Asp
NM_133497.3:c.130C>G NP_598004.1:p.His44Asp
XR_929202.1:n.631C>G
XR_929203.1:n.631C>G
NM_133497.4:c.130C>G MANE Select NP_598004.1:p.His44Asp