Canonical Allele Identifier: CA2664012167
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878575-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878575A>G , CM000664.2:g.240878575A>G GRCh38
NC_000002.11:g.241817992A>G , CM000664.1:g.241817992A>G GRCh37
NC_000002.10:g.241466665A>G NCBI36
NG_008005.1:g.14831A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-139A>G MANE Select ENSP00000302620.3:n.1072-139A>G
ENST00000307503.3:c.1072-139A>G ENSP00000302620.3:n.1072-139A>G
ENST00000470255.1:n.850-139A>G
NM_000030.2:c.1072-139A>G NP_000021.1:n.1072-139A>G
NM_000030.3:c.1072-139A>G MANE Select NP_000021.1:n.1072-139A>G
Search 100 bp 5'
Search 100 bp 3'