Canonical Allele Identifier: CA1339331000
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869326T= , CM000664.2:g.240869326T= GRCh38
NC_000002.11:g.241808743T= , CM000664.1:g.241808743T= GRCh37
NC_000002.10:g.241457416T= NCBI36
NG_008005.1:g.5582T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.322T= MANE Select ENSP00000302620.3:p.Trp108=
ENST00000307503.3:c.322T= ENSP00000302620.3:p.Trp108=
ENST00000472436.1:n.342T=
NM_000030.2:c.322T= NP_000021.1:p.Trp108=
XR_924060.1:n.405+907A=
NM_000030.3:c.322T= MANE Select NP_000021.1:p.Trp108=