Canonical Allele Identifier: CA1828287933
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717966A= , CM000671.2:g.2717966A= GRCh38
NC_000009.11:g.2717966A= , CM000671.1:g.2717966A= GRCh37
NC_000009.10:g.2707966A= NCBI36
NG_012181.1:g.5441A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.227A= MANE Select ENSP00000371514.3:p.Gln76=
ENST00000382082.3:c.227A= ENSP00000371514.3:p.Gln76=
NM_133497.3:c.227A= NP_598004.1:p.Gln76=
XR_929202.1:n.728A=
XR_929203.1:n.728A=
NM_133497.4:c.227A= MANE Select NP_598004.1:p.Gln76=