Canonical Allele Identifier: CA1339336155
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878769T= , CM000664.2:g.240878769T= GRCh38
NC_000002.11:g.241818186T= , CM000664.1:g.241818186T= GRCh37
NC_000002.10:g.241466859T= NCBI36
NG_008005.1:g.15025T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1127T= MANE Select ENSP00000302620.3:p.Val376=
ENST00000307503.3:c.1127T= ENSP00000302620.3:p.Val376=
ENST00000470255.1:n.905T=
NM_000030.2:c.1127T= NP_000021.1:p.Val376=
NM_000030.3:c.1127T= MANE Select NP_000021.1:p.Val376=