Canonical Allele Identifier: CA2209131
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs367672388
ExAC: 2:241812441 G / T
gnomAD v2: 2-241812441-G-T
gnomAD v3: 2-240873024-G-T
gnomAD v4: 2-240873024-G-T
MyVariant Identifiers: chr2:g.241812441G>T (hg19) chr2:g.240873024G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873024G>T , CM000664.2:g.240873024G>T GRCh38
NC_000002.11:g.241812441G>T , CM000664.1:g.241812441G>T GRCh37
NC_000002.10:g.241461114G>T NCBI36
NG_008005.1:g.9280G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.570G>T MANE Select ENSP00000302620.3:p.Gly190=
ENST00000307503.3:c.570G>T ENSP00000302620.3:p.Gly190=
ENST00000472436.1:n.590G>T
ENST00000476698.1:n.307G>T
NM_000030.2:c.570G>T NP_000021.1:p.Gly190=
NM_000030.3:c.570G>T MANE Select NP_000021.1:p.Gly190=
Search 100 bp 5'
Search 100 bp 3'