Canonical Allele Identifier: CA513694424
Gene: SCARF2 HGNC NCBI

Linked Data

gnomAD v4: 22-20425882-T-C
MyVariant Identifiers: chr22:g.20780169T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425882T>C , CM000684.2:g.20425882T>C GRCh38
NC_000022.10:g.20780169T>C , CM000684.1:g.20780169T>C GRCh37
NC_000022.9:g.19110169T>C NCBI36
NG_031868.2:g.16978A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2094A>G MANE Select ENSP00000477564.2:p.Lys698=
ENST00000615031.4:c.2109A>G ENSP00000479389.1:p.Lys703=
ENST00000622235.4:c.2094A>G ENSP00000477564.1:p.Lys698=
ENST00000623402.1:c.2109A>G ENSP00000485276.1:p.Lys703=
NM_153334.6:c.2109A>G NP_699165.3:p.Lys703=
NM_182895.4:c.2094A>G NP_878315.2:p.Lys698=
NM_153334.7:c.2109A>G NP_699165.3:p.Lys703=
NM_182895.5:c.2094A>G MANE Select NP_878315.2:p.Lys698=
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