Canonical Allele Identifier: CA2664004791
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240871309-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871309C>A , CM000664.2:g.240871309C>A GRCh38
NC_000002.11:g.241810726C>A , CM000664.1:g.241810726C>A GRCh37
NC_000002.10:g.241459399C>A NCBI36
NG_008005.1:g.7565C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.424-40C>A MANE Select ENSP00000302620.3:n.424-40C>A
ENST00000307503.3:c.424-40C>A ENSP00000302620.3:n.424-40C>A
ENST00000472436.1:n.444-40C>A
ENST00000476698.1:n.121C>A
NM_000030.2:c.424-40C>A NP_000021.1:n.424-40C>A
NM_000030.3:c.424-40C>A MANE Select NP_000021.1:n.424-40C>A
Search 100 bp 5'
Search 100 bp 3'