Canonical Allele Identifier: CA14531028
Gene: ABHD3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11662721

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21681452C>T , CM000680.2:g.21681452C>T GRCh38
NC_000018.8:g.17515411C>T NCBI36
NC_000018.9:g.19261413C>T , CM000680.1:g.19261413C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000289119.6:c.555+2468G>A ENSP00000289119.2:p.=
ENST00000577891.1:c.*74+2468G>A ENSP00000463365.1:p.=
ENST00000578270.5:c.-471+2468G>A ENSP00000462578.1:p.=
ENST00000579875.5:n.485-17222G>A
ENST00000580981.5:c.509+20864G>A ENSP00000462935.1:p.=
NM_001308256.1:c.509+20864G>A VV NP_001295185.1:p.=
NM_138340.4:c.555+2468G>A VV NP_612213.2:p.=
XM_011525847.1:c.555+2468G>A XP_011524149.1:p.=
XR_243847.1:n.695+2468G>A
XR_935209.1:n.650-17222G>A
XR_935210.1:n.650-17222G>A
XM_011525847.3:c.555+2468G>A
XM_017025572.1:c.-470-17222G>A XP_016881061.1:p.=
XM_017025573.1:c.-471+721G>A XP_016881062.1:p.=
XM_017025574.1:c.-471+309G>A XP_016881063.1:p.=
XM_024451094.1:c.-471+2468G>A XP_024306862.1:p.=
XR_001753151.2:n.683+2468G>A
XR_002958165.1:n.683+2468G>A
XR_935209.3:n.638-17222G>A
XR_935210.3:n.638-17222G>A