Canonical Allele Identifier: CA351318136

Gene: AGXT

Linked Data

• MyVariant Identifiers: chr2:g.241814573A>T (hg19) ; chr2:g.240875156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875156A>T , CM000664.2:g.240875156A>T	GRCh38
NC_000002.11:g.241814573A>T , CM000664.1:g.241814573A>T	GRCh37
NC_000002.10:g.241463246A>T	NCBI36
NG_008005.1:g.11412A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.728A>T MANE Select	ENSP00000302620.3:p.Asp243Val
ENST00000307503.3:c.728A>T	ENSP00000302620.3:p.Asp243Val
ENST00000476698.1:n.380A>T
NM_000030.2:c.728A>T	NP_000021.1:p.Asp243Val
NM_000030.3:c.728A>T MANE Select	NP_000021.1:p.Asp243Val