Canonical Allele Identifier: CA540535889
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1214763261
gnomAD v2: 2-241812653-T-A
gnomAD v3: 2-240873236-T-A
gnomAD v4: 2-240873236-T-A
MyVariant Identifiers: chr2:g.241812653T>A (hg19) chr2:g.240873236T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873236T>A , CM000664.2:g.240873236T>A GRCh38
NC_000002.11:g.241812653T>A , CM000664.1:g.241812653T>A GRCh37
NC_000002.10:g.241461326T>A NCBI36
NG_008005.1:g.9492T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+187T>A MANE Select ENSP00000302620.3:n.595+187T>A
ENST00000307503.3:c.595+187T>A ENSP00000302620.3:n.595+187T>A
ENST00000472436.1:n.802T>A
ENST00000476698.1:n.332+187T>A
NM_000030.2:c.595+187T>A NP_000021.1:n.595+187T>A
NM_000030.3:c.595+187T>A MANE Select NP_000021.1:n.595+187T>A
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