Canonical Allele Identifier: CA410738828

Gene: SCARF2

Linked Data

• gnomAD v4: 22-20425717-G-T
• MyVariant Identifiers: chr22:g.20780006G>T (hg19) ; chr22:g.20425717G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425717G>T , CM000684.2:g.20425717G>T	GRCh38
NC_000022.10:g.20780006G>T , CM000684.1:g.20780006G>T	GRCh37
NC_000022.9:g.19110006G>T	NCBI36
NG_031868.2:g.17143C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2259C>A MANE Select	ENSP00000477564.2:p.Pro753=
ENST00000615031.4:c.2272C>A	ENSP00000479389.1:p.His758Asn
ENST00000622235.4:c.2259C>A	ENSP00000477564.1:p.Pro753=
ENST00000623402.1:c.2274C>A	ENSP00000485276.1:p.Pro758=
NM_153334.6:c.2274C>A	NP_699165.3:p.Pro758=
NM_182895.4:c.2259C>A	NP_878315.2:p.Pro753=
NM_153334.7:c.2274C>A	NP_699165.3:p.Pro758=
NM_182895.5:c.2259C>A MANE Select	NP_878315.2:p.Pro753=