Canonical Allele Identifier: CA463853617
Gene: KCNV2 HGNC NCBI

Linked Data

gnomAD v4: 9-2718555-C-G
MyVariant Identifiers: chr9:g.2718555C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718555C>G , CM000671.2:g.2718555C>G GRCh38
NC_000009.11:g.2718555C>G , CM000671.1:g.2718555C>G GRCh37
NC_000009.10:g.2708555C>G NCBI36
NG_012181.1:g.6030C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.816C>G MANE Select ENSP00000371514.3:p.Val272=
ENST00000382082.3:c.816C>G ENSP00000371514.3:p.Val272=
NM_133497.3:c.816C>G NP_598004.1:p.Val272=
XR_929202.1:n.1317C>G
XR_929203.1:n.1317C>G
NM_133497.4:c.816C>G MANE Select NP_598004.1:p.Val272=