Canonical Allele Identifier: CA432024159
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241813432G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240874015G>A , CM000664.2:g.240874015G>A GRCh38
NC_000002.11:g.241813432G>A , CM000664.1:g.241813432G>A GRCh37
NC_000002.10:g.241462105G>A NCBI36
NG_008005.1:g.10271G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.633G>A MANE Select ENSP00000302620.3:p.Leu211=
ENST00000307503.3:c.633G>A ENSP00000302620.3:p.Leu211=
ENST00000476698.1:n.332+966G>A
NM_000030.2:c.633G>A NP_000021.1:p.Leu211=
NM_000030.3:c.633G>A MANE Select NP_000021.1:p.Leu211=
Search 100 bp 5'
Search 100 bp 3'