Canonical Allele Identifier: CA432021919
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808727T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869310T>G , CM000664.2:g.240869310T>G GRCh38
NC_000002.11:g.241808727T>G , CM000664.1:g.241808727T>G GRCh37
NC_000002.10:g.241457400T>G NCBI36
NG_008005.1:g.5566T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.306T>G MANE Select ENSP00000302620.3:p.Val102=
ENST00000307503.3:c.306T>G ENSP00000302620.3:p.Val102=
ENST00000472436.1:n.326T>G
NM_000030.2:c.306T>G NP_000021.1:p.Val102=
XR_924060.1:n.405+923A>C
NM_000030.3:c.306T>G MANE Select NP_000021.1:p.Val102=
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