Canonical Allele Identifier: CA432021861
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808709T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869292T>A , CM000664.2:g.240869292T>A GRCh38
NC_000002.11:g.241808709T>A , CM000664.1:g.241808709T>A GRCh37
NC_000002.10:g.241457382T>A NCBI36
NG_008005.1:g.5548T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.288T>A MANE Select ENSP00000302620.3:p.Pro96=
ENST00000307503.3:c.288T>A ENSP00000302620.3:p.Pro96=
ENST00000472436.1:n.308T>A
NM_000030.2:c.288T>A NP_000021.1:p.Pro96=
XR_924060.1:n.405+941A>T
NM_000030.3:c.288T>A MANE Select NP_000021.1:p.Pro96=