Canonical Allele Identifier: CA513694880
Gene: SCARF2 HGNC NCBI

Linked Data

gnomAD v4: 22-20425678-A-G
MyVariant Identifiers: chr22:g.20779968A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425678A>G , CM000684.2:g.20425678A>G GRCh38
NC_000022.10:g.20779968A>G , CM000684.1:g.20779968A>G GRCh37
NC_000022.9:g.19109968A>G NCBI36
NG_031868.2:g.17182T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2298T>C MANE Select ENSP00000477564.2:p.Ala766=
ENST00000615031.4:c.2310T>C ENSP00000479389.1:p.Ala770=
ENST00000622235.4:c.2298T>C ENSP00000477564.1:p.Ala766=
ENST00000623402.1:c.2313T>C ENSP00000485276.1:p.Ala771=
NM_153334.6:c.2313T>C NP_699165.3:p.Ala771=
NM_182895.4:c.2298T>C NP_878315.2:p.Ala766=
NM_153334.7:c.2313T>C NP_699165.3:p.Ala771=
NM_182895.5:c.2298T>C MANE Select NP_878315.2:p.Ala766=
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