Canonical Allele Identifier: CA351318206
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875174A>G , CM000664.2:g.240875174A>G GRCh38
NC_000002.11:g.241814591A>G , CM000664.1:g.241814591A>G GRCh37
NC_000002.10:g.241463264A>G NCBI36
NG_008005.1:g.11430A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.746A>G MANE Select ENSP00000302620.3:p.Asn249Ser
ENST00000307503.3:c.746A>G ENSP00000302620.3:p.Asn249Ser
ENST00000476698.1:n.398A>G
NM_000030.2:c.746A>G NP_000021.1:p.Asn249Ser
NM_000030.3:c.746A>G MANE Select NP_000021.1:p.Asn249Ser