Canonical Allele Identifier: CA463853618
Gene: KCNV2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.2718555C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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