Canonical Allele Identifier: CA14955968
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1319199
gnomAD v2: 22-20779563-C-T
gnomAD v3: 22-20425273-C-T
gnomAD v4: 22-20425273-C-T
MyVariant Identifiers: chr22:g.20779563C>T (hg19) chr22:g.20425273C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425273C>T , CM000684.2:g.20425273C>T GRCh38
NC_000022.10:g.20779563C>T , CM000684.1:g.20779563C>T GRCh37
NC_000022.9:g.19109563C>T NCBI36
NG_031868.2:g.17587G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.*102G>A MANE Select ENSP00000477564.2:n.*102G>A
ENST00000615031.4:c.*102G>A ENSP00000479389.1:n.*102G>A
ENST00000622235.4:c.*102G>A ENSP00000477564.1:n.*102G>A
ENST00000623402.1:c.*102G>A ENSP00000485276.1:n.*102G>A
NM_153334.6:c.*102G>A NP_699165.3:n.*102G>A
NM_182895.4:c.*102G>A NP_878315.2:n.*102G>A
NM_153334.7:c.*102G>A NP_699165.3:n.*102G>A
NM_182895.5:c.*102G>A MANE Select NP_878315.2:n.*102G>A
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