Canonical Allele Identifier: CA432234946
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808387T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868970T>C , CM000664.2:g.240868970T>C GRCh38
NC_000002.11:g.241808387T>C , CM000664.1:g.241808387T>C GRCh37
NC_000002.10:g.241457060T>C NCBI36
NG_008005.1:g.5226T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.105T>C MANE Select ENSP00000302620.3:p.Pro35=
ENST00000307503.3:c.105T>C ENSP00000302620.3:p.Pro35=
ENST00000472436.1:n.125T>C
NM_000030.2:c.105T>C NP_000021.1:p.Pro35=
XR_924060.1:n.405+1263A>G
NM_000030.3:c.105T>C MANE Select NP_000021.1:p.Pro35=
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