Canonical Allele Identifier: CA410739641
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20780194G>C (hg19) chr22:g.20425907G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425907G>C , CM000684.2:g.20425907G>C GRCh38
NC_000022.10:g.20780194G>C , CM000684.1:g.20780194G>C GRCh37
NC_000022.9:g.19110194G>C NCBI36
NG_031868.2:g.16953C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2069C>G MANE Select ENSP00000477564.2:p.Ala690Gly
ENST00000615031.4:c.2084C>G ENSP00000479389.1:p.Ala695Gly
ENST00000622235.4:c.2069C>G ENSP00000477564.1:p.Ala690Gly
ENST00000623402.1:c.2084C>G ENSP00000485276.1:p.Ala695Gly
NM_153334.6:c.2084C>G NP_699165.3:p.Ala695Gly
NM_182895.4:c.2069C>G NP_878315.2:p.Ala690Gly
NM_153334.7:c.2084C>G NP_699165.3:p.Ala695Gly
NM_182895.5:c.2069C>G MANE Select NP_878315.2:p.Ala690Gly
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