Canonical Allele Identifier: CA513694878
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20779968A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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