Canonical Allele Identifier: CA410738767
Gene: SCARF2 HGNC NCBI

Linked Data

gnomAD v4: 22-20425707-C-T
MyVariant Identifiers: chr22:g.20779996C>T (hg19) chr22:g.20425707C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425707C>T , CM000684.2:g.20425707C>T GRCh38
NC_000022.10:g.20779996C>T , CM000684.1:g.20779996C>T GRCh37
NC_000022.9:g.19109996C>T NCBI36
NG_031868.2:g.17153G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2269G>A MANE Select ENSP00000477564.2:p.Gly757Ser
ENST00000615031.4:c.2282G>A ENSP00000479389.1:p.Arg761Gln
ENST00000622235.4:c.2269G>A ENSP00000477564.1:p.Gly757Ser
ENST00000623402.1:c.2284G>A ENSP00000485276.1:p.Gly762Ser
NM_153334.6:c.2284G>A NP_699165.3:p.Gly762Ser
NM_182895.4:c.2269G>A NP_878315.2:p.Gly757Ser
NM_153334.7:c.2284G>A NP_699165.3:p.Gly762Ser
NM_182895.5:c.2269G>A MANE Select NP_878315.2:p.Gly757Ser
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