Canonical Allele Identifier: CA432234641
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808423G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869006G>C , CM000664.2:g.240869006G>C GRCh38
NC_000002.11:g.241808423G>C , CM000664.1:g.241808423G>C GRCh37
NC_000002.10:g.241457096G>C NCBI36
NG_008005.1:g.5262G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.141G>C MANE Select ENSP00000302620.3:p.Gly47=
ENST00000307503.3:c.141G>C ENSP00000302620.3:p.Gly47=
ENST00000472436.1:n.161G>C
NM_000030.2:c.141G>C NP_000021.1:p.Gly47=
XR_924060.1:n.405+1227C>G
NM_000030.3:c.141G>C MANE Select NP_000021.1:p.Gly47=
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