Canonical Allele Identifier: CA2578740842
Gene: ARG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573216T>C , CM000668.2:g.131573216T>C GRCh38
NC_000006.11:g.131894356T>C , CM000668.1:g.131894356T>C GRCh37
NC_000006.10:g.131936049T>C NCBI36
NG_007086.2:g.4992T>C
NG_031860.1:g.60008A>G
NG_031860.2:g.60008A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000672052.1:n.305-3447T>C
ENST00000672233.1:c.77-5895T>C ENSP00000499826.1:n.77-5895T>C
ENST00000673234.1:c.77-3447T>C ENSP00000499885.1:n.77-3447T>C
ENST00000368087.7:c.-67T>C ENSP00000357066.3:n.-67T>C
ENST00000469293.1:n.23T>C
NM_000045.3:c.-67T>C NP_000036.2:n.-67T>C
NM_001244438.1:c.-67T>C NP_001231367.1:n.-67T>C
XM_011535801.1:c.-67T>C XP_011534103.1:n.-67T>C
XM_011535801.2:c.-67T>C XP_011534103.1:n.-67T>C