Canonical Allele Identifier: CA351319232
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877588G>C , CM000664.2:g.240877588G>C GRCh38
NC_000002.11:g.241817005G>C , CM000664.1:g.241817005G>C GRCh37
NC_000002.10:g.241465678G>C NCBI36
NG_008005.1:g.13844G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.898G>C MANE Select ENSP00000302620.3:p.Gly300Arg
ENST00000307503.3:c.898G>C ENSP00000302620.3:p.Gly300Arg
ENST00000470255.1:n.676G>C
NM_000030.2:c.898G>C NP_000021.1:p.Gly300Arg
NM_000030.3:c.898G>C MANE Select NP_000021.1:p.Gly300Arg