Canonical Allele Identifier: CA10112201
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs768328788
ExAC: 22:20780077 T / A
gnomAD v2: 22-20780077-T-A
gnomAD v3: 22-20425790-T-A
gnomAD v4: 22-20425790-T-A
MyVariant Identifiers: chr22:g.20780077T>A (hg19) chr22:g.20425790T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425790T>A , CM000684.2:g.20425790T>A GRCh38
NC_000022.10:g.20780077T>A , CM000684.1:g.20780077T>A GRCh37
NC_000022.9:g.19110077T>A NCBI36
NG_031868.2:g.17070A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2186A>T MANE Select ENSP00000477564.2:p.Glu729Val
ENST00000615031.4:c.2201A>T ENSP00000479389.1:p.Glu734Val
ENST00000622235.4:c.2186A>T ENSP00000477564.1:p.Glu729Val
ENST00000623402.1:c.2201A>T ENSP00000485276.1:p.Glu734Val
NM_153334.6:c.2201A>T NP_699165.3:p.Glu734Val
NM_182895.4:c.2186A>T NP_878315.2:p.Glu729Val
NM_153334.7:c.2201A>T NP_699165.3:p.Glu734Val
NM_182895.5:c.2186A>T MANE Select NP_878315.2:p.Glu729Val
Search 100 bp 5'
Search 100 bp 3'