Canonical Allele Identifier: CA432234990
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808399A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868982A>T , CM000664.2:g.240868982A>T GRCh38
NC_000002.11:g.241808399A>T , CM000664.1:g.241808399A>T GRCh37
NC_000002.10:g.241457072A>T NCBI36
NG_008005.1:g.5238A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.117A>T MANE Select ENSP00000302620.3:p.Ala39=
ENST00000307503.3:c.117A>T ENSP00000302620.3:p.Ala39=
ENST00000472436.1:n.137A>T
NM_000030.2:c.117A>T NP_000021.1:p.Ala39=
XR_924060.1:n.405+1251T>A
NM_000030.3:c.117A>T MANE Select NP_000021.1:p.Ala39=