Canonical Allele Identifier: CA1242107450

Gene: XDH

Linked Data

• dbSNP Id: rs1685372773

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31348844A>G , CM000664.2:g.31348844A>G	GRCh38
NC_000002.11:g.31571710A>G , CM000664.1:g.31571710A>G	GRCh37
NC_000002.10:g.31425214A>G	NCBI36
NG_008871.1:g.70902T>C
NG_008871.2:g.70902T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379416.4:c.3051+55T>C MANE Select	ENSP00000368727.3:n.3051+55T>C
ENST00000379416.3:c.3051+55T>C	ENSP00000368727.3:n.3051+55T>C
NM_000379.3:c.3051+55T>C	NP_000370.2:n.3051+55T>C
XM_011533095.1:c.3048+55T>C	XP_011531397.1:n.3048+55T>C
XM_011533096.1:c.3051+55T>C	XP_011531398.1:n.3051+55T>C
XM_011533095.2:c.3048+55T>C	XP_011531397.1:n.3048+55T>C
XM_011533096.2:c.3051+55T>C	XP_011531398.1:n.3051+55T>C
NM_000379.4:c.3051+55T>C MANE Select	NP_000370.2:n.3051+55T>C