Canonical Allele Identifier: CA432234815
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808339C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868922C>A , CM000664.2:g.240868922C>A GRCh38
NC_000002.11:g.241808339C>A , CM000664.1:g.241808339C>A GRCh37
NC_000002.10:g.241457012C>A NCBI36
NG_008005.1:g.5178C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.57C>A MANE Select ENSP00000302620.3:p.Ser19=
ENST00000307503.3:c.57C>A ENSP00000302620.3:p.Ser19=
ENST00000472436.1:n.77C>A
NM_000030.2:c.57C>A NP_000021.1:p.Ser19=
XR_924060.1:n.405+1311G>T
NM_000030.3:c.57C>A MANE Select NP_000021.1:p.Ser19=
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