Canonical Allele Identifier: CA432234847
Gene: AGXT HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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