Canonical Allele Identifier: CA2664010243
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240877069-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877069G>T , CM000664.2:g.240877069G>T GRCh38
NC_000002.11:g.241816486G>T , CM000664.1:g.241816486G>T GRCh37
NC_000002.10:g.241465159G>T NCBI36
NG_008005.1:g.13325G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-468G>T MANE Select ENSP00000302620.3:n.847-468G>T
ENST00000307503.3:c.847-468G>T ENSP00000302620.3:n.847-468G>T
ENST00000470255.1:n.157G>T
NM_000030.2:c.847-468G>T NP_000021.1:n.847-468G>T
NM_000030.3:c.847-468G>T MANE Select NP_000021.1:n.847-468G>T
Search 100 bp 5'
Search 100 bp 3'