Canonical Allele Identifier: CA513694050

Gene: SCARF2

Linked Data

• dbSNP Id: rs771079357
• MyVariant Identifiers: chr22:g.20779688T>G (hg19) ; chr22:g.20425398T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425398T>G , CM000684.2:g.20425398T>G	GRCh38
NC_000022.10:g.20779688T>G , CM000684.1:g.20779688T>G	GRCh37
NC_000022.9:g.19109688T>G	NCBI36
NG_031868.2:g.17462A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2578A>C MANE Select	ENSP00000477564.2:p.Arg860=
ENST00000615031.4:c.2590A>C	ENSP00000479389.1:p.Arg864=
ENST00000622235.4:c.2578A>C	ENSP00000477564.1:p.Arg860=
ENST00000623402.1:c.2593A>C	ENSP00000485276.1:p.Arg865=
NM_153334.6:c.2593A>C	NP_699165.3:p.Arg865=
NM_182895.4:c.2578A>C	NP_878315.2:p.Arg860=
NM_153334.7:c.2593A>C	NP_699165.3:p.Arg865=
NM_182895.5:c.2578A>C MANE Select	NP_878315.2:p.Arg860=