Canonical Allele Identifier: CA2664006328
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873375-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873375G>T , CM000664.2:g.240873375G>T GRCh38
NC_000002.11:g.241812792G>T , CM000664.1:g.241812792G>T GRCh37
NC_000002.10:g.241461465G>T NCBI36
NG_008005.1:g.9631G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+326G>T MANE Select ENSP00000302620.3:n.595+326G>T
ENST00000307503.3:c.595+326G>T ENSP00000302620.3:n.595+326G>T
ENST00000472436.1:n.941G>T
ENST00000476698.1:n.332+326G>T
NM_000030.2:c.595+326G>T NP_000021.1:n.595+326G>T
NM_000030.3:c.595+326G>T MANE Select NP_000021.1:n.595+326G>T
Search 100 bp 5'
Search 100 bp 3'