Canonical Allele Identifier: CA410738293

Gene: SCARF2

Linked Data

• gnomAD v4: 22-20425539-C-A
• MyVariant Identifiers: chr22:g.20779829C>A (hg19) ; chr22:g.20425539C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425539C>A , CM000684.2:g.20425539C>A	GRCh38
NC_000022.10:g.20779829C>A , CM000684.1:g.20779829C>A	GRCh37
NC_000022.9:g.19109829C>A	NCBI36
NG_031868.2:g.17321G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000622235.5:c.2437G>T MANE Select	ENSP00000477564.2:p.Ala813Ser
ENST00000615031.4:c.2449G>T	ENSP00000479389.1:p.Ala817Ser
ENST00000622235.4:c.2437G>T	ENSP00000477564.1:p.Ala813Ser
ENST00000623402.1:c.2452G>T	ENSP00000485276.1:p.Ala818Ser
NM_153334.6:c.2452G>T	NP_699165.3:p.Ala818Ser
NM_182895.4:c.2437G>T	NP_878315.2:p.Ala813Ser
NM_153334.7:c.2452G>T	NP_699165.3:p.Ala818Ser
NM_182895.5:c.2437G>T MANE Select	NP_878315.2:p.Ala813Ser