Canonical Allele Identifier: CA351313402
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869196C>G , CM000664.2:g.240869196C>G GRCh38
NC_000002.11:g.241808613C>G , CM000664.1:g.241808613C>G GRCh37
NC_000002.10:g.241457286C>G NCBI36
NG_008005.1:g.5452C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.192C>G MANE Select ENSP00000302620.3:p.Ile64Met
ENST00000307503.3:c.192C>G ENSP00000302620.3:p.Ile64Met
ENST00000472436.1:n.212C>G
NM_000030.2:c.192C>G NP_000021.1:p.Ile64Met
XR_924060.1:n.405+1037G>C
NM_000030.3:c.192C>G MANE Select NP_000021.1:p.Ile64Met