Canonical Allele Identifier: CA432234953
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808390C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868973C>A , CM000664.2:g.240868973C>A GRCh38
NC_000002.11:g.241808390C>A , CM000664.1:g.241808390C>A GRCh37
NC_000002.10:g.241457063C>A NCBI36
NG_008005.1:g.5229C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.108C>A MANE Select ENSP00000302620.3:p.Arg36=
ENST00000307503.3:c.108C>A ENSP00000302620.3:p.Arg36=
ENST00000472436.1:n.128C>A
NM_000030.2:c.108C>A NP_000021.1:p.Arg36=
XR_924060.1:n.405+1260G>T
NM_000030.3:c.108C>A MANE Select NP_000021.1:p.Arg36=