Canonical Allele Identifier: CA2577302783
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878668A>C , CM000664.2:g.240878668A>C GRCh38
NC_000002.11:g.241818085A>C , CM000664.1:g.241818085A>C GRCh37
NC_000002.10:g.241466758A>C NCBI36
NG_008005.1:g.14924A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1072-46A>C MANE Select ENSP00000302620.3:n.1072-46A>C
ENST00000307503.3:c.1072-46A>C ENSP00000302620.3:n.1072-46A>C
ENST00000470255.1:n.850-46A>C
NM_000030.2:c.1072-46A>C NP_000021.1:n.1072-46A>C
NM_000030.3:c.1072-46A>C MANE Select NP_000021.1:n.1072-46A>C