Canonical Allele Identifier: CA777553410
Gene: ABHD3 HGNC NCBI

Linked Data

dbSNP Id: rs1255378511

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.21681536T>C , CM000680.2:g.21681536T>C GRCh38
NC_000018.9:g.19261497T>C , CM000680.1:g.19261497T>C GRCh37
NC_000018.8:g.17515495T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000289119.7:c.555+2384A>G MANE Select ENSP00000289119.2:n.555+2384A>G
ENST00000289119.6:c.555+2384A>G ENSP00000289119.2:n.555+2384A>G
ENST00000577891.1:c.*74+2384A>G ENSP00000463365.1:n.*74+2384A>G
ENST00000578270.5:c.-471+2384A>G ENSP00000462578.1:n.-471+2384A>G
ENST00000579875.5:n.485-17306A>G
ENST00000580981.5:c.509+20780A>G ENSP00000462935.1:n.509+20780A>G
NM_001308256.1:c.509+20780A>G NP_001295185.1:n.509+20780A>G
NM_138340.4:c.555+2384A>G NP_612213.2:n.555+2384A>G
XM_011525847.1:c.555+2384A>G XP_011524149.1:n.555+2384A>G
XR_243847.1:n.695+2384A>G
XR_935209.1:n.650-17306A>G
XR_935210.1:n.650-17306A>G
XM_011525847.3:c.555+2384A>G XP_011524149.1:n.555+2384A>G
XM_017025572.1:c.-470-17306A>G XP_016881061.1:n.-470-17306A>G
XM_017025573.1:c.-471+637A>G XP_016881062.1:n.-471+637A>G
XM_017025574.1:c.-471+225A>G XP_016881063.1:n.-471+225A>G
XM_024451094.1:c.-471+2384A>G XP_024306862.1:n.-471+2384A>G
XR_001753151.2:n.683+2384A>G
XR_002958165.1:n.683+2384A>G
XR_935209.3:n.638-17306A>G
XR_935210.3:n.638-17306A>G
NM_138340.5:c.555+2384A>G MANE Select NP_612213.2:n.555+2384A>G
NM_001308256.2:c.509+20780A>G NP_001295185.1:n.509+20780A>G