Canonical Allele Identifier: CA1828289315
Gene: KCNV2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2718565G= , CM000671.2:g.2718565G= GRCh38
NC_000009.11:g.2718565G= , CM000671.1:g.2718565G= GRCh37
NC_000009.10:g.2708565G= NCBI36
NG_012181.1:g.6040G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.826G= MANE Select ENSP00000371514.3:p.Ala276=
ENST00000382082.3:c.826G= ENSP00000371514.3:p.Ala276=
NM_133497.3:c.826G= NP_598004.1:p.Ala276=
XR_929202.1:n.1327G=
XR_929203.1:n.1327G=
NM_133497.4:c.826G= MANE Select NP_598004.1:p.Ala276=
Search 100 bp 5'
Search 100 bp 3'