Canonical Allele Identifier: CA410738738

Gene: SCARF2

Linked Data

• gnomAD v4: 22-20425703-C-A
• MyVariant Identifiers: chr22:g.20779992C>A (hg19) ; chr22:g.20425703C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425703C>A , CM000684.2:g.20425703C>A	GRCh38
NC_000022.10:g.20779992C>A , CM000684.1:g.20779992C>A	GRCh37
NC_000022.9:g.19109992C>A	NCBI36
NG_031868.2:g.17157G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2273G>T MANE Select	ENSP00000477564.2:p.Gly758Val
ENST00000615031.4:c.2286G>T	ENSP00000479389.1:p.Arg762=
ENST00000622235.4:c.2273G>T	ENSP00000477564.1:p.Gly758Val
ENST00000623402.1:c.2288G>T	ENSP00000485276.1:p.Gly763Val
NM_153334.6:c.2288G>T	NP_699165.3:p.Gly763Val
NM_182895.4:c.2273G>T	NP_878315.2:p.Gly758Val
NM_153334.7:c.2288G>T	NP_699165.3:p.Gly763Val
NM_182895.5:c.2273G>T MANE Select	NP_878315.2:p.Gly758Val