Canonical Allele Identifier: CA1339334160
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875105C= , CM000664.2:g.240875105C= GRCh38
NC_000002.11:g.241814522C= , CM000664.1:g.241814522C= GRCh37
NC_000002.10:g.241463195C= NCBI36
NG_008005.1:g.11361C=

Transcript Alleles

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