Canonical Allele Identifier: CA1664127869

Gene: ARG1

Linked Data

• dbSNP Id: rs1562351309
• gnomAD v4: 6-131573245-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573245C>T , CM000668.2:g.131573245C>T	GRCh38
NC_000006.11:g.131894385C>T , CM000668.1:g.131894385C>T	GRCh37
NC_000006.10:g.131936078C>T	NCBI36
NG_007086.2:g.5021C>T
NG_031860.1:g.59979G>A
NG_031860.2:g.59979G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.-38C>T MANE Select	ENSP00000357066.3:n.-38C>T
ENST00000672052.1:n.305-3418C>T
ENST00000672233.1:c.77-5866C>T	ENSP00000499826.1:n.77-5866C>T
ENST00000673234.1:c.77-3418C>T	ENSP00000499885.1:n.77-3418C>T
ENST00000673427.1:c.-38C>T	ENSP00000500160.1:n.-38C>T
ENST00000275196.5:n.20C>T
ENST00000356962.2:c.-38C>T	ENSP00000349446.2:n.-38C>T
ENST00000368087.7:c.-38C>T	ENSP00000357066.3:n.-38C>T
ENST00000469293.1:n.52C>T
ENST00000498260.1:n.4C>T
NM_000045.3:c.-38C>T	NP_000036.2:n.-38C>T
NM_001244438.1:c.-38C>T	NP_001231367.1:n.-38C>T
XM_011535801.1:c.-38C>T	XP_011534103.1:n.-38C>T
XM_011535801.2:c.-38C>T	XP_011534103.1:n.-38C>T
NM_000045.4:c.-38C>T MANE Select	NP_000036.2:n.-38C>T
NM_001244438.2:c.-38C>T	NP_001231367.1:n.-38C>T
NM_001369020.1:c.-38C>T	NP_001355949.1:n.-38C>T
NR_160934.1:n.20C>T