Canonical Allele Identifier: CA10112177
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs746996253
ExAC: 22:20779833 C / A
gnomAD v2: 22-20779833-C-A
gnomAD v4: 22-20425543-C-A
MyVariant Identifiers: chr22:g.20779833C>A (hg19) chr22:g.20425543C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425543C>A , CM000684.2:g.20425543C>A GRCh38
NC_000022.10:g.20779833C>A , CM000684.1:g.20779833C>A GRCh37
NC_000022.9:g.19109833C>A NCBI36
NG_031868.2:g.17317G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000622235.5:c.2433G>T MANE Select ENSP00000477564.2:p.Ser811=
ENST00000615031.4:c.2445G>T ENSP00000479389.1:p.Ser815=
ENST00000622235.4:c.2433G>T ENSP00000477564.1:p.Ser811=
ENST00000623402.1:c.2448G>T ENSP00000485276.1:p.Ser816=
NM_153334.6:c.2448G>T NP_699165.3:p.Ser816=
NM_182895.4:c.2433G>T NP_878315.2:p.Ser811=
NM_153334.7:c.2448G>T NP_699165.3:p.Ser816=
NM_182895.5:c.2433G>T MANE Select NP_878315.2:p.Ser811=
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