Canonical Allele Identifier: CA68173721
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs868580226

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869173A>G , CM000664.2:g.240869173A>G GRCh38
NC_000002.11:g.241808590A>G , CM000664.1:g.241808590A>G GRCh37
NC_000002.10:g.241457263A>G NCBI36
NG_008005.1:g.5429A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.169A>G MANE Select ENSP00000302620.3:p.Met57Val
ENST00000307503.3:c.169A>G ENSP00000302620.3:p.Met57Val
ENST00000472436.1:n.189A>G
NM_000030.2:c.169A>G NP_000021.1:p.Met57Val
XR_924060.1:n.405+1060T>C
NM_000030.3:c.169A>G MANE Select NP_000021.1:p.Met57Val