Canonical Allele Identifier: CA1339330828
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869046A= , CM000664.2:g.240869046A= GRCh38
NC_000002.11:g.241808463A= , CM000664.1:g.241808463A= GRCh37
NC_000002.10:g.241457136A= NCBI36
NG_008005.1:g.5302A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.165+16A= MANE Select ENSP00000302620.3:n.165+16A=
ENST00000307503.3:c.165+16A= ENSP00000302620.3:n.165+16A=
ENST00000472436.1:n.185+16A=
NM_000030.2:c.165+16A= NP_000021.1:n.165+16A=
XR_924060.1:n.405+1187T=
NM_000030.3:c.165+16A= MANE Select NP_000021.1:n.165+16A=