Canonical Allele Identifier: CA2701856543
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106429852

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873944A>G , CM000664.2:g.240873944A>G GRCh38
NC_000002.11:g.241813361A>G , CM000664.1:g.241813361A>G GRCh37
NC_000002.10:g.241462034A>G NCBI36
NG_008005.1:g.10200A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-34A>G MANE Select ENSP00000302620.3:n.596-34A>G
ENST00000307503.3:c.596-34A>G ENSP00000302620.3:n.596-34A>G
ENST00000476698.1:n.332+895A>G
NM_000030.2:c.596-34A>G NP_000021.1:n.596-34A>G
NM_000030.3:c.596-34A>G MANE Select NP_000021.1:n.596-34A>G