Canonical Allele Identifier: CA1339334299
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059018518
gnomAD v4: 2-240875353-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875353A>T , CM000664.2:g.240875353A>T GRCh38
NC_000002.11:g.241814770A>T , CM000664.1:g.241814770A>T GRCh37
NC_000002.10:g.241463443A>T NCBI36
NG_008005.1:g.11609A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+149A>T MANE Select ENSP00000302620.3:n.776+149A>T
ENST00000307503.3:c.776+149A>T ENSP00000302620.3:n.776+149A>T
ENST00000476698.1:n.428+149A>T
NM_000030.2:c.776+149A>T NP_000021.1:n.776+149A>T
NM_000030.3:c.776+149A>T MANE Select NP_000021.1:n.776+149A>T
Search 100 bp 5'
Search 100 bp 3'