Canonical Allele Identifier: CA463853635
Gene: KCNV2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2718564G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718564G>C , CM000671.2:g.2718564G>C GRCh38
NC_000009.11:g.2718564G>C , CM000671.1:g.2718564G>C GRCh37
NC_000009.10:g.2708564G>C NCBI36
NG_012181.1:g.6039G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.825G>C MANE Select ENSP00000371514.3:p.Val275=
ENST00000382082.3:c.825G>C ENSP00000371514.3:p.Val275=
NM_133497.3:c.825G>C NP_598004.1:p.Val275=
XR_929202.1:n.1326G>C
XR_929203.1:n.1326G>C
NM_133497.4:c.825G>C MANE Select NP_598004.1:p.Val275=