Canonical Allele Identifier: CA410738561
Gene: SCARF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2485140
ClinVar RCV Id: RCV003219267
dbSNP Id: rs1182875086
gnomAD v2: 22-20779939-C-T
gnomAD v3: 22-20425649-C-T
gnomAD v4: 22-20425649-C-T
MyVariant Identifiers: chr22:g.20779939C>T (hg19) chr22:g.20425649C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425649C>T , CM000684.2:g.20425649C>T GRCh38
NC_000022.10:g.20779939C>T , CM000684.1:g.20779939C>T GRCh37
NC_000022.9:g.19109939C>T NCBI36
NG_031868.2:g.17211G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2327G>A MANE Select ENSP00000477564.2:p.Gly776Asp
ENST00000615031.4:c.2339G>A ENSP00000479389.1:p.Gly780Asp
ENST00000622235.4:c.2327G>A ENSP00000477564.1:p.Gly776Asp
ENST00000623402.1:c.2342G>A ENSP00000485276.1:p.Gly781Asp
NM_153334.6:c.2342G>A NP_699165.3:p.Gly781Asp
NM_182895.4:c.2327G>A NP_878315.2:p.Gly776Asp
NM_153334.7:c.2342G>A NP_699165.3:p.Gly781Asp
NM_182895.5:c.2327G>A MANE Select NP_878315.2:p.Gly776Asp
Search 100 bp 5'
Search 100 bp 3'