Canonical Allele Identifier: CA1339335949
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059039777

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878377C>G , CM000664.2:g.240878377C>G GRCh38
NC_000002.11:g.241817794C>G , CM000664.1:g.241817794C>G GRCh37
NC_000002.10:g.241466467C>G NCBI36
NG_008005.1:g.14633C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1071+227C>G MANE Select ENSP00000302620.3:n.1071+227C>G
ENST00000307503.3:c.1071+227C>G ENSP00000302620.3:n.1071+227C>G
ENST00000470255.1:n.849+227C>G
NM_000030.2:c.1071+227C>G NP_000021.1:n.1071+227C>G
NM_000030.3:c.1071+227C>G MANE Select NP_000021.1:n.1071+227C>G