Canonical Allele Identifier: CA13590430
Gene: AGAP2 HGNC NCBI

Linked Data

dbSNP Id: rs12368653

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739473G>A , CM000674.2:g.57739473G>A GRCh38
NC_000012.11:g.58133256G>A , CM000674.1:g.58133256G>A GRCh37
NC_000012.10:g.56419523G>A NCBI36
NG_029755.1:g.7689C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257897.7:c.160+2439C>T ENSP00000257897.3:p.=
ENST00000553221.5:n.189+1272G>A
NM_014770.3:c.160+2439C>T NP_055585.1:p.=
XM_005268626.1:c.160+2439C>T XP_005268683.1:p.=
XM_005268626.2:c.160+2439C>T XP_005268683.1:p.=
NM_014770.4:c.160+2439C>T NP_055585.1:p.=