Canonical Allele Identifier: CA2576928881
Gene: XDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31348847G>C , CM000664.2:g.31348847G>C GRCh38
NC_000002.11:g.31571713G>C , CM000664.1:g.31571713G>C GRCh37
NC_000002.10:g.31425217G>C NCBI36
NG_008871.1:g.70899C>G
NG_008871.2:g.70899C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379416.4:c.3051+52C>G MANE Select ENSP00000368727.3:n.3051+52C>G
ENST00000379416.3:c.3051+52C>G ENSP00000368727.3:n.3051+52C>G
NM_000379.3:c.3051+52C>G NP_000370.2:n.3051+52C>G
XM_011533095.1:c.3048+52C>G XP_011531397.1:n.3048+52C>G
XM_011533096.1:c.3051+52C>G XP_011531398.1:n.3051+52C>G
XM_011533095.2:c.3048+52C>G XP_011531397.1:n.3048+52C>G
XM_011533096.2:c.3051+52C>G XP_011531398.1:n.3051+52C>G
NM_000379.4:c.3051+52C>G MANE Select NP_000370.2:n.3051+52C>G