Canonical Allele Identifier: CA2579810876

Gene: CBS

Linked Data

• ClinVar Variation Id: 2706104
• ClinVar RCV Id: RCV003496263

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.43072173C>T , CM000683.2:g.43072173C>T	GRCh38
NG_008938.1:g.8758G>A , LRG_777:g.8758G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398165.8:c.21G>A MANE Select	ENSP00000381231.4:p.Gln7=
ENST00000352178.9:c.21G>A	ENSP00000344460.5:p.Gln7=
ENST00000359624.7:c.21G>A	ENSP00000352643.3:p.Gln7=
ENST00000398158.5:c.21G>A	ENSP00000381225.1:p.Gln7=
ENST00000398165.7:c.21G>A	ENSP00000381231.3:p.Gln7=
ENST00000441030.5:c.21G>A	ENSP00000388235.1:p.Gln7=
ENST00000465732.5:n.200G>A
ENST00000470912.5:n.281G>A
ENST00000488526.1:n.272G>A
NM_000071.2:c.21G>A , LRG_777t1:c.21G>A	NP_000062.1:p.Gln7=
NM_001178008.1:c.21G>A	NP_001171479.1:p.Gln7=
NM_001178009.1:c.21G>A	NP_001171480.1:p.Gln7=
XM_011529777.1:c.21G>A	XP_011528079.1:p.Gln7=
XM_011529778.1:c.21G>A	XP_011528080.1:p.Gln7=
XM_011529779.1:c.21G>A	XP_011528081.1:p.Gln7=
XM_011529781.1:c.21G>A	XP_011528083.1:p.Gln7=
XM_011529782.1:c.21G>A	XP_011528084.1:p.Gln7=
NM_001178008.2:c.21G>A	NP_001171479.1:p.Gln7=
NM_001178009.2:c.21G>A	NP_001171480.1:p.Gln7=
NM_001320298.1:c.21G>A	NP_001307227.1:p.Gln7=
XM_011529777.2:c.21G>A	XP_011528079.1:p.Gln7=
XM_017028491.2:c.21G>A	XP_016883980.1:p.Gln7=
XM_024452136.1:c.-748G>A	XP_024307904.1:n.-748G>A
XM_024452137.1:c.-748G>A	XP_024307905.1:n.-748G>A
XM_024452138.1:c.-1026G>A	XP_024307906.1:n.-1026G>A
XM_024452139.1:c.-1026G>A	XP_024307907.1:n.-1026G>A
XM_024452140.1:c.-1026G>A	XP_024307908.1:n.-1026G>A
XR_001754916.2:n.171G>A
XR_001754917.2:n.171G>A
XR_002958634.1:n.171G>A
NM_000071.3:c.21G>A MANE Select	NP_000062.1:p.Gln7=
NM_001178009.3:c.21G>A	NP_001171480.1:p.Gln7=
NM_001178008.3:c.21G>A	NP_001171479.1:p.Gln7=
NM_001320298.2:c.21G>A	NP_001307227.1:p.Gln7=