Canonical Allele Identifier: CA1828287675
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717866A= , CM000671.2:g.2717866A= GRCh38
NC_000009.11:g.2717866A= , CM000671.1:g.2717866A= GRCh37
NC_000009.10:g.2707866A= NCBI36
NG_012181.1:g.5341A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382082.4:c.127A= MANE Select ENSP00000371514.3:p.Ile43=
ENST00000382082.3:c.127A= ENSP00000371514.3:p.Ile43=
NM_133497.3:c.127A= NP_598004.1:p.Ile43=
XR_929202.1:n.628A=
XR_929203.1:n.628A=
NM_133497.4:c.127A= MANE Select NP_598004.1:p.Ile43=