Canonical Allele Identifier: CA2664011784
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878018-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878018G>A , CM000664.2:g.240878018G>A GRCh38
NC_000002.11:g.241817435G>A , CM000664.1:g.241817435G>A GRCh37
NC_000002.10:g.241466108G>A NCBI36
NG_008005.1:g.14274G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.943-4G>A MANE Select ENSP00000302620.3:n.943-4G>A
ENST00000307503.3:c.943-4G>A ENSP00000302620.3:n.943-4G>A
ENST00000470255.1:n.721-4G>A
NM_000030.2:c.943-4G>A NP_000021.1:n.943-4G>A
NM_000030.3:c.943-4G>A MANE Select NP_000021.1:n.943-4G>A
Search 100 bp 5'
Search 100 bp 3'