Canonical Allele Identifier: CA322182173
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs759611
MyVariant Identifiers: chr22:g.20425657C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425657C>G , CM000684.2:g.20425657C>G GRCh38
NG_031868.2:g.17203G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2319G>C MANE Select ENSP00000477564.2:p.Glu773Asp
ENST00000615031.4:c.2331G>C ENSP00000479389.1:p.Glu777Asp
ENST00000622235.4:c.2319G>C ENSP00000477564.1:p.Glu773Asp
ENST00000623402.1:c.2334G>C ENSP00000485276.1:p.Glu778Asp
NM_153334.6:c.2334G>C NP_699165.3:p.Glu778Asp
NM_182895.4:c.2319G>C NP_878315.2:p.Glu773Asp
NM_153334.7:c.2334G>C NP_699165.3:p.Glu778Asp
NM_182895.5:c.2319G>C MANE Select NP_878315.2:p.Glu773Asp