Canonical Allele Identifier: CA351318174
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875165G>T , CM000664.2:g.240875165G>T GRCh38
NC_000002.11:g.241814582G>T , CM000664.1:g.241814582G>T GRCh37
NC_000002.10:g.241463255G>T NCBI36
NG_008005.1:g.11421G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.737G>T MANE Select ENSP00000302620.3:p.Trp246Leu
ENST00000307503.3:c.737G>T ENSP00000302620.3:p.Trp246Leu
ENST00000476698.1:n.389G>T
NM_000030.2:c.737G>T NP_000021.1:p.Trp246Leu
NM_000030.3:c.737G>T MANE Select NP_000021.1:p.Trp246Leu