Canonical Allele Identifier: CA2038156722
Gene: SUOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55996852A= , CM000674.2:g.55996852A= GRCh38
NC_000012.11:g.56390636A= , CM000674.1:g.56390636A= GRCh37
NC_000012.10:g.54676903A= NCBI36
NG_008136.1:g.4594A=

Transcript Alleles

HGVS Amino-acid Change
XM_017019905.2:c.-775A= XP_016875394.1:n.-775A=
XM_017019907.2:c.-865A= XP_016875396.1:n.-865A=
XM_024449167.1:c.-649A= XP_024304935.1:n.-649A=