Canonical Allele Identifier: CA1339334613
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875904G= , CM000664.2:g.240875904G= GRCh38
NC_000002.11:g.241815321G= , CM000664.1:g.241815321G= GRCh37
NC_000002.10:g.241463994G= NCBI36
NG_008005.1:g.12160G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.777-31G= MANE Select ENSP00000302620.3:n.777-31G=
ENST00000307503.3:c.777-31G= ENSP00000302620.3:n.777-31G=
ENST00000476698.1:n.429-31G=
NM_000030.2:c.777-31G= NP_000021.1:n.777-31G=
NM_000030.3:c.777-31G= MANE Select NP_000021.1:n.777-31G=