Canonical Allele Identifier: CA463853339
Gene: KCNV2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2717874C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717874C>A , CM000671.2:g.2717874C>A GRCh38
NC_000009.11:g.2717874C>A , CM000671.1:g.2717874C>A GRCh37
NC_000009.10:g.2707874C>A NCBI36
NG_012181.1:g.5349C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.135C>A MANE Select ENSP00000371514.3:p.Gly45=
ENST00000382082.3:c.135C>A ENSP00000371514.3:p.Gly45=
NM_133497.3:c.135C>A NP_598004.1:p.Gly45=
XR_929202.1:n.636C>A
XR_929203.1:n.636C>A
NM_133497.4:c.135C>A MANE Select NP_598004.1:p.Gly45=