Canonical Allele Identifier: CA513694172

Gene: SCARF2

Linked Data

• dbSNP Id: rs1249082562
• gnomAD v2: 22-20779800-C-T
• gnomAD v4: 22-20425510-C-T
• MyVariant Identifiers: chr22:g.20779800C>T (hg19) ; chr22:g.20425510C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425510C>T , CM000684.2:g.20425510C>T	GRCh38
NC_000022.10:g.20779800C>T , CM000684.1:g.20779800C>T	GRCh37
NC_000022.9:g.19109800C>T	NCBI36
NG_031868.2:g.17350G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2466G>A MANE Select	ENSP00000477564.2:p.Pro822=
ENST00000615031.4:c.2478G>A	ENSP00000479389.1:p.Pro826=
ENST00000622235.4:c.2466G>A	ENSP00000477564.1:p.Pro822=
ENST00000623402.1:c.2481G>A	ENSP00000485276.1:p.Pro827=
NM_153334.6:c.2481G>A	NP_699165.3:p.Pro827=
NM_182895.4:c.2466G>A	NP_878315.2:p.Pro822=
NM_153334.7:c.2481G>A	NP_699165.3:p.Pro827=
NM_182895.5:c.2466G>A MANE Select	NP_878315.2:p.Pro822=