Canonical Allele Identifier: CA432025551
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2707861
ClinVar RCV Id: RCV003545068
gnomAD v4: 2-240877608-G-A
MyVariant Identifiers: chr2:g.241817025G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877608G>A , CM000664.2:g.240877608G>A GRCh38
NC_000002.11:g.241817025G>A , CM000664.1:g.241817025G>A GRCh37
NC_000002.10:g.241465698G>A NCBI36
NG_008005.1:g.13864G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.918G>A MANE Select ENSP00000302620.3:p.Gly306=
ENST00000307503.3:c.918G>A ENSP00000302620.3:p.Gly306=
ENST00000470255.1:n.696G>A
NM_000030.2:c.918G>A NP_000021.1:p.Gly306=
NM_000030.3:c.918G>A MANE Select NP_000021.1:p.Gly306=
Search 100 bp 5'
Search 100 bp 3'