Canonical Allele Identifier: CA513694077
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20779725C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425435C>G , CM000684.2:g.20425435C>G GRCh38
NC_000022.10:g.20779725C>G , CM000684.1:g.20779725C>G GRCh37
NC_000022.9:g.19109725C>G NCBI36
NG_031868.2:g.17425G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000622235.5:c.2541G>C MANE Select ENSP00000477564.2:p.Pro847=
ENST00000615031.4:c.2553G>C ENSP00000479389.1:p.Pro851=
ENST00000622235.4:c.2541G>C ENSP00000477564.1:p.Pro847=
ENST00000623402.1:c.2556G>C ENSP00000485276.1:p.Pro852=
NM_153334.6:c.2556G>C NP_699165.3:p.Pro852=
NM_182895.4:c.2541G>C NP_878315.2:p.Pro847=
NM_153334.7:c.2556G>C NP_699165.3:p.Pro852=
NM_182895.5:c.2541G>C MANE Select NP_878315.2:p.Pro847=
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