Canonical Allele Identifier: CA432234846
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808661C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869244C>A , CM000664.2:g.240869244C>A GRCh38
NC_000002.11:g.241808661C>A , CM000664.1:g.241808661C>A GRCh37
NC_000002.10:g.241457334C>A NCBI36
NG_008005.1:g.5500C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.240C>A MANE Select ENSP00000302620.3:p.Gly80=
ENST00000307503.3:c.240C>A ENSP00000302620.3:p.Gly80=
ENST00000472436.1:n.260C>A
NM_000030.2:c.240C>A NP_000021.1:p.Gly80=
XR_924060.1:n.405+989G>T
NM_000030.3:c.240C>A MANE Select NP_000021.1:p.Gly80=