Canonical Allele Identifier: CA513694081
Gene: SCARF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.20779728C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20425438C>A , CM000684.2:g.20425438C>A GRCh38
NC_000022.10:g.20779728C>A , CM000684.1:g.20779728C>A GRCh37
NC_000022.9:g.19109728C>A NCBI36
NG_031868.2:g.17422G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000622235.5:c.2538G>T MANE Select ENSP00000477564.2:p.Pro846=
ENST00000615031.4:c.2550G>T ENSP00000479389.1:p.Pro850=
ENST00000622235.4:c.2538G>T ENSP00000477564.1:p.Pro846=
ENST00000623402.1:c.2553G>T ENSP00000485276.1:p.Pro851=
NM_153334.6:c.2553G>T NP_699165.3:p.Pro851=
NM_182895.4:c.2538G>T NP_878315.2:p.Pro846=
NM_153334.7:c.2553G>T NP_699165.3:p.Pro851=
NM_182895.5:c.2538G>T MANE Select NP_878315.2:p.Pro846=