Canonical Allele Identifier: CA1538676523

Gene: AGXT2

Linked Data

• dbSNP Id: rs1766114651

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.34998635A>T , CM000667.2:g.34998635A>T	GRCh38
NC_000005.9:g.34998740A>T , CM000667.1:g.34998740A>T	GRCh37
NC_000005.8:g.35034497A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000231420.11:c.*84T>A MANE Select	ENSP00000231420.6:n.*84T>A
ENST00000231420.10:c.*84T>A	ENSP00000231420.6:n.*84T>A
ENST00000510428.1:c.*45+39T>A	ENSP00000422799.1:n.*45+39T>A
ENST00000512135.5:n.1299T>A
ENST00000618015.4:c.*84T>A	ENSP00000479154.1:n.*84T>A
NM_001306173.1:c.*45+39T>A	NP_001293102.1:n.*45+39T>A
NM_031900.3:c.*84T>A	NP_114106.1:n.*84T>A
XM_005248337.2:c.*84T>A	XP_005248394.1:n.*84T>A
XM_005248338.2:c.*84T>A	XP_005248395.1:n.*84T>A
XM_011514077.1:c.1438-233T>A	XP_011512379.1:n.1438-233T>A
XM_005248337.3:c.*84T>A	XP_005248394.1:n.*84T>A
XM_005248338.3:c.*84T>A	XP_005248395.1:n.*84T>A
XM_017009748.2:c.*84T>A	XP_016865237.1:n.*84T>A
NM_031900.4:c.*84T>A MANE Select	NP_114106.1:n.*84T>A
NM_001306173.2:c.*45+39T>A	NP_001293102.1:n.*45+39T>A