Canonical Allele Identifier: CA2680351446
Gene: ARG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573222C>T , CM000668.2:g.131573222C>T GRCh38
NC_000006.11:g.131894362C>T , CM000668.1:g.131894362C>T GRCh37
NC_000006.10:g.131936055C>T NCBI36
NG_007086.2:g.4998C>T
NG_031860.1:g.60002G>A
NG_031860.2:g.60002G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000672052.1:n.305-3441C>T
ENST00000672233.1:c.77-5889C>T ENSP00000499826.1:n.77-5889C>T
ENST00000673234.1:c.77-3441C>T ENSP00000499885.1:n.77-3441C>T
ENST00000368087.7:c.-61C>T ENSP00000357066.3:n.-61C>T
ENST00000469293.1:n.29C>T
NM_000045.3:c.-61C>T NP_000036.2:n.-61C>T
NM_001244438.1:c.-61C>T NP_001231367.1:n.-61C>T
XM_011535801.1:c.-61C>T XP_011534103.1:n.-61C>T
XM_011535801.2:c.-61C>T XP_011534103.1:n.-61C>T