Canonical Allele Identifier: CA325105
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 212872
dbSNP Id: rs148865119
MyVariant Identifiers: chr21:g.43072048G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.43072048G>A , CM000683.2:g.43072048G>A GRCh38
NG_008938.1:g.8883C>T , LRG_777:g.8883C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000398165.8:c.146C>T MANE Select ENSP00000381231.4:p.Pro49Leu
ENST00000352178.9:c.146C>T ENSP00000344460.5:p.Pro49Leu
ENST00000359624.7:c.146C>T ENSP00000352643.3:p.Pro49Leu
ENST00000398158.5:c.146C>T ENSP00000381225.1:p.Pro49Leu
ENST00000398165.7:c.146C>T ENSP00000381231.3:p.Pro49Leu
ENST00000441030.5:c.146C>T ENSP00000388235.1:p.Pro49Leu
ENST00000465732.5:n.325C>T
ENST00000470912.5:n.406C>T
ENST00000488526.1:n.397C>T
NM_000071.2:c.146C>T , LRG_777t1:c.146C>T NP_000062.1:p.Pro49Leu
NM_001178008.1:c.146C>T NP_001171479.1:p.Pro49Leu
NM_001178009.1:c.146C>T NP_001171480.1:p.Pro49Leu
XM_011529777.1:c.146C>T XP_011528079.1:p.Pro49Leu
XM_011529778.1:c.146C>T XP_011528080.1:p.Pro49Leu
XM_011529779.1:c.146C>T XP_011528081.1:p.Pro49Leu
XM_011529781.1:c.146C>T XP_011528083.1:p.Pro49Leu
XM_011529782.1:c.146C>T XP_011528084.1:p.Pro49Leu
NM_001178008.2:c.146C>T NP_001171479.1:p.Pro49Leu
NM_001178009.2:c.146C>T NP_001171480.1:p.Pro49Leu
NM_001320298.1:c.146C>T NP_001307227.1:p.Pro49Leu
XM_011529777.2:c.146C>T XP_011528079.1:p.Pro49Leu
XM_017028491.2:c.146C>T XP_016883980.1:p.Pro49Leu
XM_024452136.1:c.-623C>T XP_024307904.1:n.-623C>T
XM_024452137.1:c.-623C>T XP_024307905.1:n.-623C>T
XM_024452138.1:c.-901C>T XP_024307906.1:n.-901C>T
XM_024452139.1:c.-901C>T XP_024307907.1:n.-901C>T
XM_024452140.1:c.-901C>T XP_024307908.1:n.-901C>T
XR_001754916.2:n.296C>T
XR_001754917.2:n.296C>T
XR_002958634.1:n.296C>T
NM_000071.3:c.146C>T MANE Select NP_000062.1:p.Pro49Leu
NM_001178009.3:c.146C>T NP_001171480.1:p.Pro49Leu
NM_001178008.3:c.146C>T NP_001171479.1:p.Pro49Leu
NM_001320298.2:c.146C>T NP_001307227.1:p.Pro49Leu