Canonical Allele Identifier: CA2580068013
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2132817
ClinVar RCV Id: RCV003040637

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869155A>G , CM000664.2:g.240869155A>G GRCh38
NC_000002.11:g.241808572A>G , CM000664.1:g.241808572A>G GRCh37
NC_000002.10:g.241457245A>G NCBI36
NG_008005.1:g.5411A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-15A>G MANE Select ENSP00000302620.3:n.166-15A>G
ENST00000307503.3:c.166-15A>G ENSP00000302620.3:n.166-15A>G
ENST00000472436.1:n.186-15A>G
NM_000030.2:c.166-15A>G NP_000021.1:n.166-15A>G
XR_924060.1:n.405+1078T>C
NM_000030.3:c.166-15A>G MANE Select NP_000021.1:n.166-15A>G