Canonical Allele Identifier: CA2674368581

Gene: ARSB

Linked Data

• gnomAD v4: 5-78964644-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78964644A>G , CM000667.2:g.78964644A>G	GRCh38
NC_000005.9:g.78260467A>G , CM000667.1:g.78260467A>G	GRCh37
NC_000005.8:g.78296223A>G	NCBI36
NG_007089.1:g.26891T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264914.10:c.500-38T>C MANE Select	ENSP00000264914.4:n.500-38T>C
ENST00000565165.2:c.500-38T>C	ENSP00000456339.2:n.500-38T>C
ENST00000264914.8:c.500-38T>C	ENSP00000264914.4:n.500-38T>C
ENST00000396151.7:c.500-38T>C	ENSP00000379455.3:n.500-38T>C
ENST00000565165.1:c.500-38T>C	ENSP00000456339.1:n.500-38T>C
NM_000046.3:c.500-38T>C	NP_000037.2:n.500-38T>C
NM_198709.2:c.500-38T>C	NP_942002.1:n.500-38T>C
XM_005248506.3:c.500-38T>C	XP_005248563.1:n.500-38T>C
XM_006714615.2:c.500-38T>C	XP_006714678.1:n.500-38T>C
XM_011543390.1:c.500-38T>C	XP_011541692.1:n.500-38T>C
XM_011543391.1:c.500-38T>C	XP_011541693.1:n.500-38T>C
XM_011543392.1:c.500-38T>C	XP_011541694.1:n.500-38T>C
XM_011543393.1:c.500-38T>C	XP_011541695.1:n.500-38T>C
NM_000046.4:c.500-38T>C	NP_000037.2:n.500-38T>C
XM_011543391.3:c.500-38T>C	XP_011541693.1:n.500-38T>C
XM_011543392.3:c.500-38T>C	XP_011541694.1:n.500-38T>C
XM_011543393.2:c.500-38T>C	XP_011541695.1:n.500-38T>C
XM_017009471.2:c.500-38T>C	XP_016864960.1:n.500-38T>C
XR_001742065.2:n.571-38T>C
XR_001742066.2:n.571-38T>C
NM_000046.5:c.500-38T>C MANE Select	NP_000037.2:n.500-38T>C
NM_198709.3:c.500-38T>C	NP_942002.1:n.500-38T>C