Canonical Allele Identifier: CA1828287943

Gene: KCNV2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2717970G= , CM000671.2:g.2717970G=	GRCh38
NC_000009.11:g.2717970G= , CM000671.1:g.2717970G=	GRCh37
NC_000009.10:g.2707970G=	NCBI36
NG_012181.1:g.5445G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382082.4:c.231G= MANE Select	ENSP00000371514.3:p.Gln77=
ENST00000382082.3:c.231G=	ENSP00000371514.3:p.Gln77=
NM_133497.3:c.231G=	NP_598004.1:p.Gln77=
XR_929202.1:n.732G=
XR_929203.1:n.732G=
NM_133497.4:c.231G= MANE Select	NP_598004.1:p.Gln77=