Canonical Allele Identifier: CA1339335778
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878076A= , CM000664.2:g.240878076A= GRCh38
NC_000002.11:g.241817493A= , CM000664.1:g.241817493A= GRCh37
NC_000002.10:g.241466166A= NCBI36
NG_008005.1:g.14332A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.997A= MANE Select ENSP00000302620.3:p.Arg333=
ENST00000307503.3:c.997A= ENSP00000302620.3:p.Arg333=
ENST00000470255.1:n.775A=
NM_000030.2:c.997A= NP_000021.1:p.Arg333=
NM_000030.3:c.997A= MANE Select NP_000021.1:p.Arg333=