Canonical Allele Identifier: CA2664013960
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879194-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879194G>T , CM000664.2:g.240879194G>T GRCh38
NC_000002.11:g.241818611G>T , CM000664.1:g.241818611G>T GRCh37
NC_000002.10:g.241467284G>T NCBI36
NG_008005.1:g.15450G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*373G>T MANE Select ENSP00000302620.3:n.*373G>T
ENST00000470255.1:n.1330G>T
NM_000030.3:c.*373G>T MANE Select NP_000021.1:n.*373G>T
Search 100 bp 5'
Search 100 bp 3'