Canonical Allele Identifier: CA1557703728
Gene: ARSB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.78968999C= , CM000667.2:g.78968999C= GRCh38
NC_000005.9:g.78264822C= , CM000667.1:g.78264822C= GRCh37
NC_000005.8:g.78300578C= NCBI36
NG_007089.1:g.22536G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264914.10:c.499+7G= MANE Select ENSP00000264914.4:n.499+7G=
ENST00000565165.2:c.499+7G= ENSP00000456339.2:n.499+7G=
ENST00000264914.8:c.499+7G= ENSP00000264914.4:n.499+7G=
ENST00000396151.7:c.499+7G= ENSP00000379455.3:n.499+7G=
ENST00000565165.1:c.499+7G= ENSP00000456339.1:n.499+7G=
NM_000046.3:c.499+7G= NP_000037.2:n.499+7G=
NM_198709.2:c.499+7G= NP_942002.1:n.499+7G=
XM_005248506.3:c.499+7G= XP_005248563.1:n.499+7G=
XM_006714615.2:c.499+7G= XP_006714678.1:n.499+7G=
XM_011543390.1:c.499+7G= XP_011541692.1:n.499+7G=
XM_011543391.1:c.499+7G= XP_011541693.1:n.499+7G=
XM_011543392.1:c.499+7G= XP_011541694.1:n.499+7G=
XM_011543393.1:c.499+7G= XP_011541695.1:n.499+7G=
NM_000046.4:c.499+7G= NP_000037.2:n.499+7G=
XM_011543391.3:c.499+7G= XP_011541693.1:n.499+7G=
XM_011543392.3:c.499+7G= XP_011541694.1:n.499+7G=
XM_011543393.2:c.499+7G= XP_011541695.1:n.499+7G=
XM_017009471.2:c.499+7G= XP_016864960.1:n.499+7G=
XR_001742065.2:n.570+7G=
XR_001742066.2:n.570+7G=
NM_000046.5:c.499+7G= MANE Select NP_000037.2:n.499+7G=
NM_198709.3:c.499+7G= NP_942002.1:n.499+7G=