Canonical Allele Identifier: CA360338745
Gene: ARSB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.78839426A>T , CM000667.2:g.78839426A>T GRCh38
NC_000005.9:g.78135249A>T , CM000667.1:g.78135249A>T GRCh37
NC_000005.8:g.78171005A>T NCBI36
NG_007089.1:g.152109T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264914.10:c.1143T>A MANE Select ENSP00000264914.4:p.Ser381Arg
ENST00000264914.8:c.1143T>A ENSP00000264914.4:p.Ser381Arg
ENST00000396151.7:c.1143T>A ENSP00000379455.3:p.Ser381Arg
ENST00000565165.1:c.1143T>A ENSP00000456339.1:p.Ser381Arg
NM_000046.3:c.1143T>A NP_000037.2:p.Ser381Arg
NM_198709.2:c.1143T>A NP_942002.1:p.Ser381Arg
XM_005248506.3:c.1143T>A XP_005248563.1:p.Ser381Arg
XM_011543390.1:c.1143T>A XP_011541692.1:p.Ser381Arg
XM_011543391.1:c.1143T>A XP_011541693.1:p.Ser381Arg
XM_011543392.1:c.1143T>A XP_011541694.1:p.Ser381Arg
NM_000046.4:c.1143T>A NP_000037.2:p.Ser381Arg
XM_011543391.3:c.1143T>A XP_011541693.1:p.Ser381Arg
XM_011543392.3:c.1143T>A XP_011541694.1:p.Ser381Arg
XM_017009471.2:c.1143T>A XP_016864960.1:p.Ser381Arg
XR_001742065.2:n.1214T>A
XR_001742066.2:n.1214T>A
NM_000046.5:c.1143T>A MANE Select NP_000037.2:p.Ser381Arg
NM_198709.3:c.1143T>A NP_942002.1:p.Ser381Arg