Canonical Allele Identifier: CA751516954
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1406105168
MyVariant Identifiers: chr22:g.20425684G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425684G>C , CM000684.2:g.20425684G>C GRCh38
NG_031868.2:g.17176C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2292C>G MANE Select ENSP00000477564.2:p.Pro764=
ENST00000615031.4:c.2305-1C>G ENSP00000479389.1:n.2305-1C>G
ENST00000622235.4:c.2292C>G ENSP00000477564.1:p.Pro764=
ENST00000623402.1:c.2307C>G ENSP00000485276.1:p.Pro769=
NM_153334.6:c.2307C>G NP_699165.3:p.Pro769=
NM_182895.4:c.2292C>G NP_878315.2:p.Pro764=
NM_153334.7:c.2307C>G NP_699165.3:p.Pro769=
NM_182895.5:c.2292C>G MANE Select NP_878315.2:p.Pro764=