Canonical Allele Identifier: CA2391104986
Gene: CBS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43068445C= , CM000683.2:g.43068445C= GRCh38
NG_008938.1:g.12486G= , LRG_777:g.12486G=

Transcript Alleles

HGVS Amino-acid change
ENST00000398165.8:c.316+64G= MANE Select ENSP00000381231.4:n.316+64G=
ENST00000352178.9:c.316+64G= ENSP00000344460.5:n.316+64G=
ENST00000359624.7:c.316+64G= ENSP00000352643.3:n.316+64G=
ENST00000398158.5:c.316+64G= ENSP00000381225.1:n.316+64G=
ENST00000398165.7:c.316+64G= ENSP00000381231.3:n.316+64G=
ENST00000441030.5:c.316+64G= ENSP00000388235.1:n.316+64G=
ENST00000465732.5:n.559G=
ENST00000470912.5:n.576+64G=
ENST00000488526.1:n.631G=
NM_000071.2:c.316+64G= , LRG_777t1:c.316+64G= NP_000062.1:n.316+64G=
NM_001178008.1:c.316+64G= NP_001171479.1:n.316+64G=
NM_001178009.1:c.316+64G= NP_001171480.1:n.316+64G=
XM_011529777.1:c.316+64G= XP_011528079.1:n.316+64G=
XM_011529778.1:c.316+64G= XP_011528080.1:n.316+64G=
XM_011529779.1:c.316+64G= XP_011528081.1:n.316+64G=
XM_011529781.1:c.316+64G= XP_011528083.1:n.316+64G=
XM_011529782.1:c.316+64G= XP_011528084.1:n.316+64G=
NM_001178008.2:c.316+64G= NP_001171479.1:n.316+64G=
NM_001178009.2:c.316+64G= NP_001171480.1:n.316+64G=
NM_001320298.1:c.316+64G= NP_001307227.1:n.316+64G=
XM_011529777.2:c.316+64G= XP_011528079.1:n.316+64G=
XM_017028491.2:c.316+64G= XP_016883980.1:n.316+64G=
XM_024452136.1:c.-389G= XP_024307904.1:n.-389G=
XM_024452137.1:c.-389G= XP_024307905.1:n.-389G=
XM_024452138.1:c.-667G= XP_024307906.1:n.-667G=
XM_024452139.1:c.-667G= XP_024307907.1:n.-667G=
XM_024452140.1:c.-667G= XP_024307908.1:n.-667G=
XR_001754916.2:n.466+64G=
XR_001754917.2:n.466+64G=
XR_002958634.1:n.466+64G=
NM_000071.3:c.316+64G= MANE Select NP_000062.1:n.316+64G=
NM_001178009.3:c.316+64G= NP_001171480.1:n.316+64G=
NM_001178008.3:c.316+64G= NP_001171479.1:n.316+64G=
NM_001320298.2:c.316+64G= NP_001307227.1:n.316+64G=