Canonical Allele Identifier: CA410739139

Gene: SCARF2

Linked Data

• MyVariant Identifiers: chr22:g.20780072T>A (hg19) ; chr22:g.20425785T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425785T>A , CM000684.2:g.20425785T>A	GRCh38
NC_000022.10:g.20780072T>A , CM000684.1:g.20780072T>A	GRCh37
NC_000022.9:g.19110072T>A	NCBI36
NG_031868.2:g.17075A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2191A>T MANE Select	ENSP00000477564.2:p.Thr731Ser
ENST00000615031.4:c.2206A>T	ENSP00000479389.1:p.Thr736Ser
ENST00000622235.4:c.2191A>T	ENSP00000477564.1:p.Thr731Ser
ENST00000623402.1:c.2206A>T	ENSP00000485276.1:p.Thr736Ser
NM_153334.6:c.2206A>T	NP_699165.3:p.Thr736Ser
NM_182895.4:c.2191A>T	NP_878315.2:p.Thr731Ser
NM_153334.7:c.2206A>T	NP_699165.3:p.Thr736Ser
NM_182895.5:c.2191A>T MANE Select	NP_878315.2:p.Thr731Ser