Canonical Allele Identifier: CA2680351443
Gene: ARG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573220C>A , CM000668.2:g.131573220C>A GRCh38
NC_000006.11:g.131894360C>A , CM000668.1:g.131894360C>A GRCh37
NC_000006.10:g.131936053C>A NCBI36
NG_007086.2:g.4996C>A
NG_031860.1:g.60004G>T
NG_031860.2:g.60004G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000672052.1:n.305-3443C>A
ENST00000672233.1:c.77-5891C>A ENSP00000499826.1:n.77-5891C>A
ENST00000673234.1:c.77-3443C>A ENSP00000499885.1:n.77-3443C>A
ENST00000368087.7:c.-63C>A ENSP00000357066.3:n.-63C>A
ENST00000469293.1:n.27C>A
NM_000045.3:c.-63C>A NP_000036.2:n.-63C>A
NM_001244438.1:c.-63C>A NP_001231367.1:n.-63C>A
XM_011535801.1:c.-63C>A XP_011534103.1:n.-63C>A
XM_011535801.2:c.-63C>A XP_011534103.1:n.-63C>A