Canonical Allele Identifier: CA513694844

Gene: SCARF2

Linked Data

• dbSNP Id: rs1418677391
• gnomAD v3: 22-20425668-A-G
• gnomAD v4: 22-20425668-A-G
• MyVariant Identifiers: chr22:g.20779958A>G (hg19) ; chr22:g.20425668A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425668A>G , CM000684.2:g.20425668A>G	GRCh38
NC_000022.10:g.20779958A>G , CM000684.1:g.20779958A>G	GRCh37
NC_000022.9:g.19109958A>G	NCBI36
NG_031868.2:g.17192T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2308T>C MANE Select	ENSP00000477564.2:p.Leu770=
ENST00000615031.4:c.2320T>C	ENSP00000479389.1:p.Leu774=
ENST00000622235.4:c.2308T>C	ENSP00000477564.1:p.Leu770=
ENST00000623402.1:c.2323T>C	ENSP00000485276.1:p.Leu775=
NM_153334.6:c.2323T>C	NP_699165.3:p.Leu775=
NM_182895.4:c.2308T>C	NP_878315.2:p.Leu770=
NM_153334.7:c.2323T>C	NP_699165.3:p.Leu775=
NM_182895.5:c.2308T>C MANE Select	NP_878315.2:p.Leu770=