Canonical Allele Identifier: CA2208981
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs769473982

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868988G>C , CM000664.2:g.240868988G>C GRCh38
NC_000002.11:g.241808405G>C , CM000664.1:g.241808405G>C GRCh37
NC_000002.10:g.241457078G>C NCBI36
NG_008005.1:g.5244G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.123G>C MANE Select ENSP00000302620.3:p.Gly41=
ENST00000307503.3:c.123G>C ENSP00000302620.3:p.Gly41=
ENST00000472436.1:n.143G>C
NM_000030.2:c.123G>C NP_000021.1:p.Gly41=
XR_924060.1:n.405+1245C>G
NM_000030.3:c.123G>C MANE Select NP_000021.1:p.Gly41=