Canonical Allele Identifier: CA1828287938
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717968C= , CM000671.2:g.2717968C= GRCh38
NC_000009.11:g.2717968C= , CM000671.1:g.2717968C= GRCh37
NC_000009.10:g.2707968C= NCBI36
NG_012181.1:g.5443C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.229C= MANE Select ENSP00000371514.3:p.Gln77=
ENST00000382082.3:c.229C= ENSP00000371514.3:p.Gln77=
NM_133497.3:c.229C= NP_598004.1:p.Gln77=
XR_929202.1:n.730C=
XR_929203.1:n.730C=
NM_133497.4:c.229C= MANE Select NP_598004.1:p.Gln77=