Canonical Allele Identifier: CA432025464
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240877590-G-A
MyVariant Identifiers: chr2:g.241817007G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877590G>A , CM000664.2:g.240877590G>A GRCh38
NC_000002.11:g.241817007G>A , CM000664.1:g.241817007G>A GRCh37
NC_000002.10:g.241465680G>A NCBI36
NG_008005.1:g.13846G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.900G>A MANE Select ENSP00000302620.3:p.Gly300=
ENST00000307503.3:c.900G>A ENSP00000302620.3:p.Gly300=
ENST00000470255.1:n.678G>A
NM_000030.2:c.900G>A NP_000021.1:p.Gly300=
NM_000030.3:c.900G>A MANE Select NP_000021.1:p.Gly300=
Search 100 bp 5'
Search 100 bp 3'