Canonical Allele Identifier: CA513695011

Gene: SCARF2

Linked Data

• dbSNP Id: rs1366731629
• gnomAD v3: 22-20425740-G-T
• gnomAD v4: 22-20425740-G-T
• MyVariant Identifiers: chr22:g.20780028G>T (hg19) ; chr22:g.20425740G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425740G>T , CM000684.2:g.20425740G>T	GRCh38
NC_000022.10:g.20780028G>T , CM000684.1:g.20780028G>T	GRCh37
NC_000022.9:g.19110028G>T	NCBI36
NG_031868.2:g.17120C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2236C>A MANE Select	ENSP00000477564.2:p.Arg746Ser
ENST00000615031.4:c.2250C>A	ENSP00000479389.1:p.Ala750=
ENST00000622235.4:c.2236C>A	ENSP00000477564.1:p.Arg746Ser
ENST00000623402.1:c.2251C>A	ENSP00000485276.1:p.Arg751Ser
NM_153334.6:c.2251C>A	NP_699165.3:p.Arg751Ser
NM_182895.4:c.2236C>A	NP_878315.2:p.Arg746Ser
NM_153334.7:c.2251C>A	NP_699165.3:p.Arg751Ser
NM_182895.5:c.2236C>A MANE Select	NP_878315.2:p.Arg746Ser