Canonical Allele Identifier: CA1339334149
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875085C= , CM000664.2:g.240875085C= GRCh38
NC_000002.11:g.241814502C= , CM000664.1:g.241814502C= GRCh37
NC_000002.10:g.241463175C= NCBI36
NG_008005.1:g.11341C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-24C= MANE Select ENSP00000302620.3:n.681-24C=
ENST00000307503.3:c.681-24C= ENSP00000302620.3:n.681-24C=
ENST00000476698.1:n.333-24C=
NM_000030.2:c.681-24C= NP_000021.1:n.681-24C=
NM_000030.3:c.681-24C= MANE Select NP_000021.1:n.681-24C=