Canonical Allele Identifier: CA1339330735
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868872T= , CM000664.2:g.240868872T= GRCh38
NC_000002.11:g.241808289T= , CM000664.1:g.241808289T= GRCh37
NC_000002.10:g.241456962T= NCBI36
NG_008005.1:g.5128T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.7T= MANE Select ENSP00000302620.3:p.Ser3=
ENST00000307503.3:c.7T= ENSP00000302620.3:p.Ser3=
ENST00000472436.1:n.27T=
NM_000030.2:c.7T= NP_000021.1:p.Ser3=
XR_924060.1:n.405+1361A=
NM_000030.3:c.7T= MANE Select NP_000021.1:p.Ser3=