Canonical Allele Identifier: CA322181498
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1046828109
MyVariant Identifiers: chr22:g.20425293C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425293C>T , CM000684.2:g.20425293C>T GRCh38
NC_000022.10:g.20779583C>T , CM000684.1:g.20779583C>T GRCh37
NC_000022.9:g.19109583C>T NCBI36
NG_031868.2:g.17567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.*82G>A MANE Select ENSP00000477564.2:n.*82G>A
ENST00000615031.4:c.*82G>A ENSP00000479389.1:n.*82G>A
ENST00000622235.4:c.*82G>A ENSP00000477564.1:n.*82G>A
ENST00000623402.1:c.*82G>A ENSP00000485276.1:n.*82G>A
NM_153334.6:c.*82G>A NP_699165.3:n.*82G>A
NM_182895.4:c.*82G>A NP_878315.2:n.*82G>A
NM_153334.7:c.*82G>A NP_699165.3:n.*82G>A
NM_182895.5:c.*82G>A MANE Select NP_878315.2:n.*82G>A