Canonical Allele Identifier: CA10612915
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 335298
ClinVar RCV Id: RCV000384042
dbSNP Id: rs886055841
gnomAD v2: 2-241817008-C-T
gnomAD v3: 2-240877591-C-T
gnomAD v4: 2-240877591-C-T
MyVariant Identifiers: chr2:g.241817008C>T (hg19) chr2:g.240877591C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877591C>T , CM000664.2:g.240877591C>T GRCh38
NC_000002.11:g.241817008C>T , CM000664.1:g.241817008C>T GRCh37
NC_000002.10:g.241465681C>T NCBI36
NG_008005.1:g.13847C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.901C>T MANE Select ENSP00000302620.3:p.Arg301Cys
ENST00000307503.3:c.901C>T ENSP00000302620.3:p.Arg301Cys
ENST00000470255.1:n.679C>T
NM_000030.2:c.901C>T NP_000021.1:p.Arg301Cys
NM_000030.3:c.901C>T MANE Select NP_000021.1:p.Arg301Cys
Search 100 bp 5'
Search 100 bp 3'