Canonical Allele Identifier: CA351313961
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869350G>C , CM000664.2:g.240869350G>C GRCh38
NC_000002.11:g.241808767G>C , CM000664.1:g.241808767G>C GRCh37
NC_000002.10:g.241457440G>C NCBI36
NG_008005.1:g.5606G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.346G>C MANE Select ENSP00000302620.3:p.Gly116Arg
ENST00000307503.3:c.346G>C ENSP00000302620.3:p.Gly116Arg
ENST00000472436.1:n.366G>C
NM_000030.2:c.346G>C NP_000021.1:p.Gly116Arg
XR_924060.1:n.405+883C>G
NM_000030.3:c.346G>C MANE Select NP_000021.1:p.Gly116Arg