Canonical Allele Identifier: CA560770440

Gene: ARSB

Linked Data

• dbSNP Id: rs1279469131
• gnomAD v2: 5-78181134-A-G
• gnomAD v3: 5-78885311-A-G
• gnomAD v4: 5-78885311-A-G
• MyVariant Identifiers: chr5:g.78181134A>G (hg19) ; chr5:g.78885311A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78885311A>G , CM000667.2:g.78885311A>G	GRCh38
NC_000005.9:g.78181134A>G , CM000667.1:g.78181134A>G	GRCh37
NC_000005.8:g.78216890A>G	NCBI36
NG_007089.1:g.106224T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264914.10:c.1142+273T>C MANE Select	ENSP00000264914.4:n.1142+273T>C
ENST00000521800.2:n.325-183T>C
ENST00000565165.2:c.*218T>C	ENSP00000456339.2:n.*218T>C
ENST00000264914.8:c.1142+273T>C	ENSP00000264914.4:n.1142+273T>C
ENST00000396151.7:c.1142+273T>C	ENSP00000379455.3:n.1142+273T>C
ENST00000521800.1:n.248-183T>C
ENST00000565165.1:c.1142+273T>C	ENSP00000456339.1:n.1142+273T>C
NM_000046.3:c.1142+273T>C	NP_000037.2:n.1142+273T>C
NM_198709.2:c.1142+273T>C	NP_942002.1:n.1142+273T>C
XM_005248506.3:c.1142+273T>C	XP_005248563.1:n.1142+273T>C
XM_011543390.1:c.1142+273T>C	XP_011541692.1:n.1142+273T>C
XM_011543391.1:c.1142+273T>C	XP_011541693.1:n.1142+273T>C
XM_011543392.1:c.1142+273T>C	XP_011541694.1:n.1142+273T>C
XM_011543393.1:c.1143-183T>C	XP_011541695.1:n.1143-183T>C
NM_000046.4:c.1142+273T>C	NP_000037.2:n.1142+273T>C
XM_011543391.3:c.1142+273T>C	XP_011541693.1:n.1142+273T>C
XM_011543392.3:c.1142+273T>C	XP_011541694.1:n.1142+273T>C
XM_011543393.2:c.1143-183T>C	XP_011541695.1:n.1143-183T>C
XM_017009471.2:c.1142+273T>C	XP_016864960.1:n.1142+273T>C
XR_001742065.2:n.1213+273T>C
XR_001742066.2:n.1213+273T>C
NM_000046.5:c.1142+273T>C MANE Select	NP_000037.2:n.1142+273T>C
NM_198709.3:c.1142+273T>C	NP_942002.1:n.1142+273T>C