Canonical Allele Identifier: CA410739122
Gene: SCARF2 HGNC NCBI

Linked Data

dbSNP Id: rs1205129102
gnomAD v2: 22-20780068-G-T
gnomAD v3: 22-20425781-G-T
gnomAD v4: 22-20425781-G-T
MyVariant Identifiers: chr22:g.20780068G>T (hg19) chr22:g.20425781G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425781G>T , CM000684.2:g.20425781G>T GRCh38
NC_000022.10:g.20780068G>T , CM000684.1:g.20780068G>T GRCh37
NC_000022.9:g.19110068G>T NCBI36
NG_031868.2:g.17079C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2195C>A MANE Select ENSP00000477564.2:p.Ala732Asp
ENST00000615031.4:c.2210C>A ENSP00000479389.1:p.Ala737Asp
ENST00000622235.4:c.2195C>A ENSP00000477564.1:p.Ala732Asp
ENST00000623402.1:c.2210C>A ENSP00000485276.1:p.Ala737Asp
NM_153334.6:c.2210C>A NP_699165.3:p.Ala737Asp
NM_182895.4:c.2195C>A NP_878315.2:p.Ala732Asp
NM_153334.7:c.2210C>A NP_699165.3:p.Ala737Asp
NM_182895.5:c.2195C>A MANE Select NP_878315.2:p.Ala732Asp
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