Canonical Allele Identifier: CA351318148
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875159T>G , CM000664.2:g.240875159T>G GRCh38
NC_000002.11:g.241814576T>G , CM000664.1:g.241814576T>G GRCh37
NC_000002.10:g.241463249T>G NCBI36
NG_008005.1:g.11415T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.731T>G MANE Select ENSP00000302620.3:p.Ile244Ser
ENST00000307503.3:c.731T>G ENSP00000302620.3:p.Ile244Ser
ENST00000476698.1:n.383T>G
NM_000030.2:c.731T>G NP_000021.1:p.Ile244Ser
NM_000030.3:c.731T>G MANE Select NP_000021.1:p.Ile244Ser