Canonical Allele Identifier: CA410738630
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20425683C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425683C>T , CM000684.2:g.20425683C>T GRCh38
NC_000022.10:g.20779973C>T , CM000684.1:g.20779973C>T GRCh37
NC_000022.9:g.19109973C>T NCBI36
NG_031868.2:g.17177G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2293G>A MANE Select ENSP00000477564.2:p.Glu765Lys
ENST00000615031.4:c.2305G>A ENSP00000479389.1:p.Glu769Lys
ENST00000622235.4:c.2293G>A ENSP00000477564.1:p.Glu765Lys
ENST00000623402.1:c.2308G>A ENSP00000485276.1:p.Glu770Lys
NM_153334.6:c.2308G>A NP_699165.3:p.Glu770Lys
NM_182895.4:c.2293G>A NP_878315.2:p.Glu765Lys
NM_153334.7:c.2308G>A NP_699165.3:p.Glu770Lys
NM_182895.5:c.2293G>A MANE Select NP_878315.2:p.Glu765Lys