Canonical Allele Identifier: CA12208502
Gene: ARG1 HGNC NCBI
COSMIC:
COSN14977140 (not active)
COSN18013879 (not active)
MyVariant.info:
GRCh38 chr6:g.131570680A>G
GRCh37 chr6:g.131891820A>G
gnomAD v2:
6:131891820 A / G
gnomAD v3:
6:131570680 A / G
gnomAD v4:
chr6-131570680-A-G
Joint Max Group AF 0.63809588 (AFR)
Genomes Max Group AF 0.63809588 (AFR)
dbSNP:
2781659
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131570680A>G , CM000668.2:g.131570680A>G GRCh38
NC_000006.11:g.131891820A>G , CM000668.1:g.131891820A>G GRCh37
NC_000006.10:g.131933513A>G NCBI36
NG_007086.2:g.2456A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000672052.1:n.305-5983A>G
ENST00000672233.1:c.77-8431A>G ENSP00000499826.1:n.77-8431A>G
ENST00000673234.1:c.77-5983A>G ENSP00000499885.1:n.77-5983A>G
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