Canonical Allele Identifier: CA1603223069
Gene: SNCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.176621218G= , CM000667.2:g.176621218G= GRCh38
NC_000005.9:g.176048219G= , CM000667.1:g.176048219G= GRCh37
NC_000005.8:g.175980825G= NCBI36
NG_012131.1:g.14339C=

Transcript Alleles

HGVS Amino-acid change
ENST00000393693.7:c.368C= MANE Select ENSP00000377296.2:p.Pro123=
ENST00000310112.7:c.368C= ENSP00000308057.3:p.Pro123=
ENST00000393693.6:c.368C= ENSP00000377296.2:p.Pro123=
ENST00000506696.1:c.368C= ENSP00000422223.1:p.Pro123=
ENST00000508006.1:n.965C=
ENST00000510387.5:c.368C= ENSP00000424073.1:p.Pro123=
ENST00000614675.4:c.326C= ENSP00000479489.1:p.Pro109=
NM_001001502.1:c.368C= NP_001001502.1:p.Pro123=
NM_003085.3:c.368C= NP_003076.1:p.Pro123=
XM_006714914.2:c.368C= XP_006714977.1:p.Pro123=
XM_006714915.2:c.368C= XP_006714978.1:p.Pro123=
XM_006714916.1:c.368C= XP_006714979.1:p.Pro123=
XM_011534640.1:c.368C= XP_011532942.1:p.Pro123=
NM_001001502.2:c.368C= NP_001001502.1:p.Pro123=
NM_001318034.1:c.326C= NP_001304963.1:p.Pro109=
NM_001318035.1:c.283-375C= NP_001304964.1:n.283-375C=
NM_001318036.1:c.326C= NP_001304965.1:p.Pro109=
NM_001318037.1:c.283-375C= NP_001304966.1:n.283-375C=
NM_001363140.1:c.368C= NP_001350069.1:p.Pro123=
NM_003085.4:c.368C= NP_003076.1:p.Pro123=
XM_006714914.3:c.368C= XP_006714977.1:p.Pro123=
XM_006714915.3:c.368C= XP_006714978.1:p.Pro123=
XM_006714916.3:c.368C= XP_006714979.1:p.Pro123=
XM_011534640.2:c.368C= XP_011532942.1:p.Pro123=
NM_003085.5:c.368C= MANE Select NP_003076.1:p.Pro123=
NM_001001502.3:c.368C= NP_001001502.1:p.Pro123=
NM_001318035.2:c.283-375C= NP_001304964.1:n.283-375C=
NM_001318036.2:c.326C= NP_001304965.1:p.Pro109=
NM_001318037.2:c.283-375C= NP_001304966.1:n.283-375C=
NM_001363140.2:c.368C= NP_001350069.1:p.Pro123=
NM_001318034.2:c.326C= NP_001304963.1:p.Pro109=