Canonical Allele Identifier: CA1339336307
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879098A= , CM000664.2:g.240879098A= GRCh38
NC_000002.11:g.241818515A= , CM000664.1:g.241818515A= GRCh37
NC_000002.10:g.241467188A= NCBI36
NG_008005.1:g.15354A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*277A= MANE Select ENSP00000302620.3:n.*277A=
ENST00000307503.3:c.*277A= ENSP00000302620.3:n.*277A=
ENST00000470255.1:n.1234A=
NM_000030.2:c.*277A= NP_000021.1:n.*277A=
NM_000030.3:c.*277A= MANE Select NP_000021.1:n.*277A=