Canonical Allele Identifier: CA351319193
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877579T>G , CM000664.2:g.240877579T>G GRCh38
NC_000002.11:g.241816996T>G , CM000664.1:g.241816996T>G GRCh37
NC_000002.10:g.241465669T>G NCBI36
NG_008005.1:g.13835T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.889T>G MANE Select ENSP00000302620.3:p.Tyr297Asp
ENST00000307503.3:c.889T>G ENSP00000302620.3:p.Tyr297Asp
ENST00000470255.1:n.667T>G
NM_000030.2:c.889T>G NP_000021.1:p.Tyr297Asp
NM_000030.3:c.889T>G MANE Select NP_000021.1:p.Tyr297Asp