Canonical Allele Identifier: CA351316505
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1193697283

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240872984A>G , CM000664.2:g.240872984A>G GRCh38
NC_000002.11:g.241812401A>G , CM000664.1:g.241812401A>G GRCh37
NC_000002.10:g.241461074A>G NCBI36
NG_008005.1:g.9240A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.530A>G MANE Select ENSP00000302620.3:p.Lys177Arg
ENST00000307503.3:c.530A>G ENSP00000302620.3:p.Lys177Arg
ENST00000472436.1:n.550A>G
ENST00000476698.1:n.267A>G
NM_000030.2:c.530A>G NP_000021.1:p.Lys177Arg
NM_000030.3:c.530A>G MANE Select NP_000021.1:p.Lys177Arg