Canonical Allele Identifier: CA513694640
Gene: SCARF2 HGNC NCBI

Linked Data

gnomAD v4: 22-20425612-C-G
MyVariant Identifiers: chr22:g.20779902C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425612C>G , CM000684.2:g.20425612C>G GRCh38
NC_000022.10:g.20779902C>G , CM000684.1:g.20779902C>G GRCh37
NC_000022.9:g.19109902C>G NCBI36
NG_031868.2:g.17248G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000622235.5:c.2364G>C MANE Select ENSP00000477564.2:p.Leu788=
ENST00000615031.4:c.2376G>C ENSP00000479389.1:p.Leu792=
ENST00000622235.4:c.2364G>C ENSP00000477564.1:p.Leu788=
ENST00000623402.1:c.2379G>C ENSP00000485276.1:p.Leu793=
NM_153334.6:c.2379G>C NP_699165.3:p.Leu793=
NM_182895.4:c.2364G>C NP_878315.2:p.Leu788=
NM_153334.7:c.2379G>C NP_699165.3:p.Leu793=
NM_182895.5:c.2364G>C MANE Select NP_878315.2:p.Leu788=
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