Canonical Allele Identifier: CA513694329

Gene: SCARF2

Linked Data

• MyVariant Identifiers: chr22:g.20780139C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425852C>G , CM000684.2:g.20425852C>G	GRCh38
NC_000022.10:g.20780139C>G , CM000684.1:g.20780139C>G	GRCh37
NC_000022.9:g.19110139C>G	NCBI36
NG_031868.2:g.17008G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2124G>C MANE Select	ENSP00000477564.2:p.Thr708=
ENST00000615031.4:c.2139G>C	ENSP00000479389.1:p.Thr713=
ENST00000622235.4:c.2124G>C	ENSP00000477564.1:p.Thr708=
ENST00000623402.1:c.2139G>C	ENSP00000485276.1:p.Thr713=
NM_153334.6:c.2139G>C	NP_699165.3:p.Thr713=
NM_182895.4:c.2124G>C	NP_878315.2:p.Thr708=
NM_153334.7:c.2139G>C	NP_699165.3:p.Thr713=
NM_182895.5:c.2124G>C MANE Select	NP_878315.2:p.Thr708=