Canonical Allele Identifier: CA6093951

Gene: SLC22A20P

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65217636G>A , CM000673.2:g.65217636G>A	GRCh38
NC_000011.9:g.64985107G>A , CM000673.1:g.64985107G>A	GRCh37
NC_000011.8:g.64741683G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525264.5:n.612G>A
ENST00000525437.5:n.620G>A
ENST00000529062.5:n.584G>A
ENST00000530038.5:n.587G>A
NM_001004326.4:c.587G>A	NP_001004326.4:p.Arg196Gln
NR_033396.1:n.620G>A
XM_011545043.1:c.587G>A	XP_011543345.1:p.Arg196Gln