Canonical Allele Identifier: CA513694791
Gene: SCARF2 HGNC NCBI

Linked Data

gnomAD v4: 22-20425651-G-C
MyVariant Identifiers: chr22:g.20779941G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425651G>C , CM000684.2:g.20425651G>C GRCh38
NC_000022.10:g.20779941G>C , CM000684.1:g.20779941G>C GRCh37
NC_000022.9:g.19109941G>C NCBI36
NG_031868.2:g.17209C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2325C>G MANE Select ENSP00000477564.2:p.Arg775=
ENST00000615031.4:c.2337C>G ENSP00000479389.1:p.Arg779=
ENST00000622235.4:c.2325C>G ENSP00000477564.1:p.Arg775=
ENST00000623402.1:c.2340C>G ENSP00000485276.1:p.Arg780=
NM_153334.6:c.2340C>G NP_699165.3:p.Arg780=
NM_182895.4:c.2325C>G NP_878315.2:p.Arg775=
NM_153334.7:c.2340C>G NP_699165.3:p.Arg780=
NM_182895.5:c.2325C>G MANE Select NP_878315.2:p.Arg775=
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