Canonical Allele Identifier: CA322181561
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs778314445
gnomAD v2: 22-20779618-C-G
gnomAD v3: 22-20425328-C-G
gnomAD v4: 22-20425328-C-G
MyVariant Identifiers: chr22:g.20779618C>G (hg19) chr22:g.20425328C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425328C>G , CM000684.2:g.20425328C>G GRCh38
NC_000022.10:g.20779618C>G , CM000684.1:g.20779618C>G GRCh37
NC_000022.9:g.19109618C>G NCBI36
NG_031868.2:g.17532G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.*47G>C MANE Select ENSP00000477564.2:n.*47G>C
ENST00000615031.4:c.*47G>C ENSP00000479389.1:n.*47G>C
ENST00000622235.4:c.*47G>C ENSP00000477564.1:n.*47G>C
ENST00000623402.1:c.*47G>C ENSP00000485276.1:n.*47G>C
NM_153334.6:c.*47G>C NP_699165.3:n.*47G>C
NM_182895.4:c.*47G>C NP_878315.2:n.*47G>C
NM_153334.7:c.*47G>C NP_699165.3:n.*47G>C
NM_182895.5:c.*47G>C MANE Select NP_878315.2:n.*47G>C
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