Canonical Allele Identifier: CA68181220
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs182421127
gnomAD v3: 2-240879155-G-A
gnomAD v4: 2-240879155-G-A
MyVariant Identifiers: chr2:g.241818572G>A (hg19) chr2:g.240879155G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879155G>A , CM000664.2:g.240879155G>A GRCh38
NC_000002.11:g.241818572G>A , CM000664.1:g.241818572G>A GRCh37
NC_000002.10:g.241467245G>A NCBI36
NG_008005.1:g.15411G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*334G>A MANE Select ENSP00000302620.3:n.*334G>A
ENST00000470255.1:n.1291G>A
NM_000030.3:c.*334G>A MANE Select NP_000021.1:n.*334G>A
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