Canonical Allele Identifier: CA1339334138
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875068A= , CM000664.2:g.240875068A= GRCh38
NC_000002.11:g.241814485A= , CM000664.1:g.241814485A= GRCh37
NC_000002.10:g.241463158A= NCBI36
NG_008005.1:g.11324A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-41A= MANE Select ENSP00000302620.3:n.681-41A=
ENST00000307503.3:c.681-41A= ENSP00000302620.3:n.681-41A=
ENST00000476698.1:n.333-41A=
NM_000030.2:c.681-41A= NP_000021.1:n.681-41A=
NM_000030.3:c.681-41A= MANE Select NP_000021.1:n.681-41A=