Canonical Allele Identifier: CA10112209
Gene: SCARF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1475348
ClinVar RCV Id: RCV001976169
dbSNP Id: rs755214686
ExAC: 22:20780090 C / T
gnomAD v2: 22-20780090-C-T
gnomAD v3: 22-20425803-C-T
gnomAD v4: 22-20425803-C-T
MyVariant Identifiers: chr22:g.20780090C>T (hg19) chr22:g.20780090_20780092delinsTCG (hg19) chr22:g.20425803C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425803C>T , CM000684.2:g.20425803C>T GRCh38
NC_000022.10:g.20780090C>T , CM000684.1:g.20780090C>T GRCh37
NC_000022.9:g.19110090C>T NCBI36
NG_031868.2:g.17057G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2173G>A MANE Select ENSP00000477564.2:p.Gly725Arg
ENST00000615031.4:c.2188G>A ENSP00000479389.1:p.Gly730Arg
ENST00000622235.4:c.2173G>A ENSP00000477564.1:p.Gly725Arg
ENST00000623402.1:c.2188G>A ENSP00000485276.1:p.Gly730Arg
NM_153334.6:c.2188G>A NP_699165.3:p.Gly730Arg
NM_182895.4:c.2173G>A NP_878315.2:p.Gly725Arg
NM_153334.7:c.2188G>A NP_699165.3:p.Gly730Arg
NM_182895.5:c.2173G>A MANE Select NP_878315.2:p.Gly725Arg
Search 100 bp 5'
Search 100 bp 3'