Canonical Allele Identifier: CA1339336110
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878701C= , CM000664.2:g.240878701C= GRCh38
NC_000002.11:g.241818118C= , CM000664.1:g.241818118C= GRCh37
NC_000002.10:g.241466791C= NCBI36
NG_008005.1:g.14957C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072-13C= MANE Select ENSP00000302620.3:n.1072-13C=
ENST00000307503.3:c.1072-13C= ENSP00000302620.3:n.1072-13C=
ENST00000470255.1:n.850-13C=
NM_000030.2:c.1072-13C= NP_000021.1:n.1072-13C=
NM_000030.3:c.1072-13C= MANE Select NP_000021.1:n.1072-13C=