Canonical Allele Identifier: CA147890858
Gene: ARG1 HGNC NCBI

Linked Data

dbSNP Id: rs1028910953
gnomAD v2: 6-131894359-G-A
gnomAD v3: 6-131573219-G-A
gnomAD v4: 6-131573219-G-A
MyVariant Identifiers: chr6:g.131894359G>A (hg19) chr6:g.131573219G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573219G>A , CM000668.2:g.131573219G>A GRCh38
NC_000006.11:g.131894359G>A , CM000668.1:g.131894359G>A GRCh37
NC_000006.10:g.131936052G>A NCBI36
NG_007086.2:g.4995G>A
NG_031860.1:g.60005C>T
NG_031860.2:g.60005C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000672052.1:n.305-3444G>A
ENST00000672233.1:c.77-5892G>A ENSP00000499826.1:n.77-5892G>A
ENST00000673234.1:c.77-3444G>A ENSP00000499885.1:n.77-3444G>A
ENST00000368087.7:c.-64G>A ENSP00000357066.3:n.-64G>A
ENST00000469293.1:n.26G>A
NM_000045.3:c.-64G>A NP_000036.2:n.-64G>A
NM_001244438.1:c.-64G>A NP_001231367.1:n.-64G>A
XM_011535801.1:c.-64G>A XP_011534103.1:n.-64G>A
XM_011535801.2:c.-64G>A XP_011534103.1:n.-64G>A
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