Canonical Allele Identifier: CA2664007407
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873862-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873862G>T , CM000664.2:g.240873862G>T GRCh38
NC_000002.11:g.241813279G>T , CM000664.1:g.241813279G>T GRCh37
NC_000002.10:g.241461952G>T NCBI36
NG_008005.1:g.10118G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-116G>T MANE Select ENSP00000302620.3:n.596-116G>T
ENST00000307503.3:c.596-116G>T ENSP00000302620.3:n.596-116G>T
ENST00000476698.1:n.332+813G>T
NM_000030.2:c.596-116G>T NP_000021.1:n.596-116G>T
NM_000030.3:c.596-116G>T MANE Select NP_000021.1:n.596-116G>T
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