Canonical Allele Identifier: CA2664013733
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879137-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879137T>C , CM000664.2:g.240879137T>C GRCh38
NC_000002.11:g.241818554T>C , CM000664.1:g.241818554T>C GRCh37
NC_000002.10:g.241467227T>C NCBI36
NG_008005.1:g.15393T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*316T>C MANE Select ENSP00000302620.3:n.*316T>C
ENST00000470255.1:n.1273T>C
NM_000030.3:c.*316T>C MANE Select NP_000021.1:n.*316T>C
Search 100 bp 5'
Search 100 bp 3'