Canonical Allele Identifier: CA351312489
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868869G>C , CM000664.2:g.240868869G>C GRCh38
NC_000002.11:g.241808286G>C , CM000664.1:g.241808286G>C GRCh37
NC_000002.10:g.241456959G>C NCBI36
NG_008005.1:g.5125G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.4G>C MANE Select ENSP00000302620.3:p.Ala2Pro
ENST00000307503.3:c.4G>C ENSP00000302620.3:p.Ala2Pro
ENST00000472436.1:n.24G>C
NM_000030.2:c.4G>C NP_000021.1:p.Ala2Pro
XR_924060.1:n.405+1364C>G
NM_000030.3:c.4G>C MANE Select NP_000021.1:p.Ala2Pro