Canonical Allele Identifier: CA372795768
Gene: KCNV2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717870A>C , CM000671.2:g.2717870A>C GRCh38
NC_000009.11:g.2717870A>C , CM000671.1:g.2717870A>C GRCh37
NC_000009.10:g.2707870A>C NCBI36
NG_012181.1:g.5345A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.131A>C MANE Select ENSP00000371514.3:p.His44Pro
ENST00000382082.3:c.131A>C ENSP00000371514.3:p.His44Pro
NM_133497.3:c.131A>C NP_598004.1:p.His44Pro
XR_929202.1:n.632A>C
XR_929203.1:n.632A>C
NM_133497.4:c.131A>C MANE Select NP_598004.1:p.His44Pro