Canonical Allele Identifier: CA2664013736
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879138-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879138G>T , CM000664.2:g.240879138G>T GRCh38
NC_000002.11:g.241818555G>T , CM000664.1:g.241818555G>T GRCh37
NC_000002.10:g.241467228G>T NCBI36
NG_008005.1:g.15394G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*317G>T MANE Select ENSP00000302620.3:n.*317G>T
ENST00000470255.1:n.1274G>T
NM_000030.3:c.*317G>T MANE Select NP_000021.1:n.*317G>T
Search 100 bp 5'
Search 100 bp 3'