Canonical Allele Identifier: CA540539072
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1420774038
gnomAD v2: 2-241818566-A-G
gnomAD v3: 2-240879149-A-G
gnomAD v4: 2-240879149-A-G
MyVariant Identifiers: chr2:g.241818566A>G (hg19) chr2:g.240879149A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879149A>G , CM000664.2:g.240879149A>G GRCh38
NC_000002.11:g.241818566A>G , CM000664.1:g.241818566A>G GRCh37
NC_000002.10:g.241467239A>G NCBI36
NG_008005.1:g.15405A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*328A>G MANE Select ENSP00000302620.3:n.*328A>G
ENST00000470255.1:n.1285A>G
NM_000030.3:c.*328A>G MANE Select NP_000021.1:n.*328A>G
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