Canonical Allele Identifier: CA1242107415

Gene: XDH

Linked Data

• dbSNP Id: rs1685371029

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31348779A>C , CM000664.2:g.31348779A>C	GRCh38
NC_000002.11:g.31571645A>C , CM000664.1:g.31571645A>C	GRCh37
NC_000002.10:g.31425149A>C	NCBI36
NG_008871.1:g.70967T>G
NG_008871.2:g.70967T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379416.4:c.3051+120T>G MANE Select	ENSP00000368727.3:n.3051+120T>G
ENST00000379416.3:c.3051+120T>G	ENSP00000368727.3:n.3051+120T>G
NM_000379.3:c.3051+120T>G	NP_000370.2:n.3051+120T>G
XM_011533095.1:c.3048+120T>G	XP_011531397.1:n.3048+120T>G
XM_011533096.1:c.3051+120T>G	XP_011531398.1:n.3051+120T>G
XM_011533095.2:c.3048+120T>G	XP_011531397.1:n.3048+120T>G
XM_011533096.2:c.3051+120T>G	XP_011531398.1:n.3051+120T>G
NM_000379.4:c.3051+120T>G MANE Select	NP_000370.2:n.3051+120T>G