Canonical Allele Identifier: CA540538866
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs367933811

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878710C>A , CM000664.2:g.240878710C>A GRCh38
NC_000002.11:g.241818127C>A , CM000664.1:g.241818127C>A GRCh37
NC_000002.10:g.241466800C>A NCBI36
NG_008005.1:g.14966C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-4C>A MANE Select ENSP00000302620.3:n.1072-4C>A
ENST00000307503.3:c.1072-4C>A ENSP00000302620.3:n.1072-4C>A
ENST00000470255.1:n.850-4C>A
NM_000030.2:c.1072-4C>A NP_000021.1:n.1072-4C>A
NM_000030.3:c.1072-4C>A MANE Select NP_000021.1:n.1072-4C>A