Canonical Allele Identifier: CA351312464
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868867T>G , CM000664.2:g.240868867T>G GRCh38
NC_000002.11:g.241808284T>G , CM000664.1:g.241808284T>G GRCh37
NC_000002.10:g.241456957T>G NCBI36
NG_008005.1:g.5123T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.2T>G MANE Select ENSP00000302620.3:p.Met1Arg
ENST00000307503.3:c.2T>G ENSP00000302620.3:p.Met1Arg
ENST00000472436.1:n.22T>G
NM_000030.2:c.2T>G NP_000021.1:p.Met1Arg
XR_924060.1:n.405+1366A>C
NM_000030.3:c.2T>G MANE Select NP_000021.1:p.Met1Arg