Canonical Allele Identifier: CA410737665
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20779729G>C (hg19) chr22:g.20425439G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425439G>C , CM000684.2:g.20425439G>C GRCh38
NC_000022.10:g.20779729G>C , CM000684.1:g.20779729G>C GRCh37
NC_000022.9:g.19109729G>C NCBI36
NG_031868.2:g.17421C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2537C>G MANE Select ENSP00000477564.2:p.Pro846Arg
ENST00000615031.4:c.2549C>G ENSP00000479389.1:p.Pro850Arg
ENST00000622235.4:c.2537C>G ENSP00000477564.1:p.Pro846Arg
ENST00000623402.1:c.2552C>G ENSP00000485276.1:p.Pro851Arg
NM_153334.6:c.2552C>G NP_699165.3:p.Pro851Arg
NM_182895.4:c.2537C>G NP_878315.2:p.Pro846Arg
NM_153334.7:c.2552C>G NP_699165.3:p.Pro851Arg
NM_182895.5:c.2537C>G MANE Select NP_878315.2:p.Pro846Arg
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