Canonical Allele Identifier: CA351319874
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878798C>T , CM000664.2:g.240878798C>T GRCh38
NC_000002.11:g.241818215C>T , CM000664.1:g.241818215C>T GRCh37
NC_000002.10:g.241466888C>T NCBI36
NG_008005.1:g.15054C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1156C>T MANE Select ENSP00000302620.3:p.His386Tyr
ENST00000307503.3:c.1156C>T ENSP00000302620.3:p.His386Tyr
ENST00000470255.1:n.934C>T
NM_000030.2:c.1156C>T NP_000021.1:p.His386Tyr
NM_000030.3:c.1156C>T MANE Select NP_000021.1:p.His386Tyr