Canonical Allele Identifier: CA14967808
Gene: APOL2 HGNC NCBI

Linked Data

dbSNP Id: rs2003813

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36232947C>T , CM000684.2:g.36232947C>T GRCh38
NC_000022.10:g.36628993C>T , CM000684.1:g.36628993C>T GRCh37
NC_000022.9:g.34958939C>T NCBI36
NG_023229.2:g.12008G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358502.10:c.10+206G>A MANE Select ENSP00000351292.5:n.10+206G>A
ENST00000249066.10:c.10+206G>A ENSP00000249066.6:n.10+206G>A
ENST00000358502.9:c.10+206G>A ENSP00000351292.5:n.10+206G>A
ENST00000451256.6:c.346+206G>A ENSP00000403153.2:n.346+206G>A
ENST00000454728.5:c.10+206G>A ENSP00000400486.1:n.10+206G>A
ENST00000529194.5:c.10+206G>A ENSP00000431231.1:n.10+206G>A
NM_030882.3:c.10+206G>A NP_112092.2:n.10+206G>A
NM_145637.2:c.10+206G>A NP_663612.2:n.10+206G>A
XM_011530074.1:c.10+206G>A XP_011528376.1:n.10+206G>A
XM_011530075.1:c.10+206G>A XP_011528377.1:n.10+206G>A
XM_011530076.1:c.10+206G>A XP_011528378.1:n.10+206G>A
XM_011530077.1:c.10+206G>A XP_011528379.1:n.10+206G>A
XM_011530078.1:c.10+206G>A XP_011528380.1:n.10+206G>A
XM_011530076.3:c.10+206G>A XP_011528378.1:n.10+206G>A
XM_011530077.3:c.10+206G>A XP_011528379.1:n.10+206G>A
XM_017028724.1:c.346+206G>A XP_016884213.1:n.346+206G>A
NM_030882.4:c.10+206G>A MANE Select NP_112092.2:n.10+206G>A
NM_145637.3:c.10+206G>A NP_663612.2:n.10+206G>A