Canonical Allele Identifier: CA410737705
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20779733T>G (hg19) chr22:g.20425443T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425443T>G , CM000684.2:g.20425443T>G GRCh38
NC_000022.10:g.20779733T>G , CM000684.1:g.20779733T>G GRCh37
NC_000022.9:g.19109733T>G NCBI36
NG_031868.2:g.17417A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2533A>C MANE Select ENSP00000477564.2:p.Lys845Gln
ENST00000615031.4:c.2545A>C ENSP00000479389.1:p.Lys849Gln
ENST00000622235.4:c.2533A>C ENSP00000477564.1:p.Lys845Gln
ENST00000623402.1:c.2548A>C ENSP00000485276.1:p.Lys850Gln
NM_153334.6:c.2548A>C NP_699165.3:p.Lys850Gln
NM_182895.4:c.2533A>C NP_878315.2:p.Lys845Gln
NM_153334.7:c.2548A>C NP_699165.3:p.Lys850Gln
NM_182895.5:c.2533A>C MANE Select NP_878315.2:p.Lys845Gln
Search 100 bp 5'
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