Canonical Allele Identifier: CA10112148
Gene: SCARF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2242957
ClinVar RCV Id: RCV002732636
dbSNP Id: rs778152234

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425463C>T , CM000684.2:g.20425463C>T GRCh38
NC_000022.10:g.20779753C>T , CM000684.1:g.20779753C>T GRCh37
NC_000022.9:g.19109753C>T NCBI36
NG_031868.2:g.17397G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2513G>A MANE Select ENSP00000477564.2:p.Arg838Gln
ENST00000615031.4:c.2525G>A ENSP00000479389.1:p.Arg842Gln
ENST00000622235.4:c.2513G>A ENSP00000477564.1:p.Arg838Gln
ENST00000623402.1:c.2528G>A ENSP00000485276.1:p.Arg843Gln
NM_153334.6:c.2528G>A NP_699165.3:p.Arg843Gln
NM_182895.4:c.2513G>A NP_878315.2:p.Arg838Gln
NM_153334.7:c.2528G>A NP_699165.3:p.Arg843Gln
NM_182895.5:c.2513G>A MANE Select NP_878315.2:p.Arg838Gln