Canonical Allele Identifier: CA2209388
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs180177156

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878128G>T , CM000664.2:g.240878128G>T GRCh38
NC_000002.11:g.241817545G>T , CM000664.1:g.241817545G>T GRCh37
NC_000002.10:g.241466218G>T NCBI36
NG_008005.1:g.14384G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1049G>T MANE Select ENSP00000302620.3:p.Gly350Val
ENST00000307503.3:c.1049G>T ENSP00000302620.3:p.Gly350Val
ENST00000470255.1:n.827G>T
NM_000030.2:c.1049G>T NP_000021.1:p.Gly350Val
NM_000030.3:c.1049G>T MANE Select NP_000021.1:p.Gly350Val