Canonical Allele Identifier: CA410739568

Gene: SCARF2

Linked Data

• gnomAD v4: 22-20425890-T-C
• MyVariant Identifiers: chr22:g.20780177T>C (hg19) ; chr22:g.20425890T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425890T>C , CM000684.2:g.20425890T>C	GRCh38
NC_000022.10:g.20780177T>C , CM000684.1:g.20780177T>C	GRCh37
NC_000022.9:g.19110177T>C	NCBI36
NG_031868.2:g.16970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2086A>G MANE Select	ENSP00000477564.2:p.Lys696Glu
ENST00000615031.4:c.2101A>G	ENSP00000479389.1:p.Lys701Glu
ENST00000622235.4:c.2086A>G	ENSP00000477564.1:p.Lys696Glu
ENST00000623402.1:c.2101A>G	ENSP00000485276.1:p.Lys701Glu
NM_153334.6:c.2101A>G	NP_699165.3:p.Lys701Glu
NM_182895.4:c.2086A>G	NP_878315.2:p.Lys696Glu
NM_153334.7:c.2101A>G	NP_699165.3:p.Lys701Glu
NM_182895.5:c.2086A>G MANE Select	NP_878315.2:p.Lys696Glu