Canonical Allele Identifier: CA351318196
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1575710627

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875173A>C , CM000664.2:g.240875173A>C GRCh38
NC_000002.11:g.241814590A>C , CM000664.1:g.241814590A>C GRCh37
NC_000002.10:g.241463263A>C NCBI36
NG_008005.1:g.11429A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.745A>C MANE Select ENSP00000302620.3:p.Asn249His
ENST00000307503.3:c.745A>C ENSP00000302620.3:p.Asn249His
ENST00000476698.1:n.397A>C
NM_000030.2:c.745A>C NP_000021.1:p.Asn249His
NM_000030.3:c.745A>C MANE Select NP_000021.1:p.Asn249His