Canonical Allele Identifier: CA513695019

Gene: SCARF2

Linked Data

• MyVariant Identifiers: chr22:g.20780030C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425743C>T , CM000684.2:g.20425743C>T	GRCh38
NC_000022.10:g.20780030C>T , CM000684.1:g.20780030C>T	GRCh37
NC_000022.9:g.19110030C>T	NCBI36
NG_031868.2:g.17117G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2233G>A MANE Select	ENSP00000477564.2:p.Gly745Ser
ENST00000615031.4:c.2248-1G>A	ENSP00000479389.1:n.2248-1G>A
ENST00000622235.4:c.2233G>A	ENSP00000477564.1:p.Gly745Ser
ENST00000623402.1:c.2248G>A	ENSP00000485276.1:p.Gly750Ser
NM_153334.6:c.2248G>A	NP_699165.3:p.Gly750Ser
NM_182895.4:c.2233G>A	NP_878315.2:p.Gly745Ser
NM_153334.7:c.2248G>A	NP_699165.3:p.Gly750Ser
NM_182895.5:c.2233G>A MANE Select	NP_878315.2:p.Gly745Ser