Canonical Allele Identifier: CA1339335786
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878091T= , CM000664.2:g.240878091T= GRCh38
NC_000002.11:g.241817508T= , CM000664.1:g.241817508T= GRCh37
NC_000002.10:g.241466181T= NCBI36
NG_008005.1:g.14347T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1012T= MANE Select ENSP00000302620.3:p.Tyr338=
ENST00000307503.3:c.1012T= ENSP00000302620.3:p.Tyr338=
ENST00000470255.1:n.790T=
NM_000030.2:c.1012T= NP_000021.1:p.Tyr338=
NM_000030.3:c.1012T= MANE Select NP_000021.1:p.Tyr338=