Canonical Allele Identifier: CA101496569

Gene: SNCA

Linked Data

• dbSNP Id: rs560589322
• gnomAD v3: 4-89718416-G-C
• gnomAD v4: 4-89718416-G-C
• MyVariant Identifiers: chr4:g.90639567G>C (hg19) ; chr4:g.89718416G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89718416G>C , CM000666.2:g.89718416G>C	GRCh38
NC_000004.11:g.90639567G>C , CM000666.1:g.90639567G>C	GRCh37
NC_000004.10:g.90858590G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000673902.1:c.390+10778C>G	ENSP00000501102.1:n.390+10778C>G
XR_938982.1:n.3490-1410G>C
XR_938984.1:n.2890-1410G>C
XR_938985.1:n.1922-1410G>C
XR_938986.1:n.556-1410G>C
XR_938987.1:n.810-1410G>C
XR_938988.1:n.676-1410G>C
XR_938989.1:n.332-1410G>C
XR_938990.1:n.420-1410G>C
XR_938991.1:n.435-1410G>C
XR_938993.1:n.437-1410G>C
XR_938994.1:n.901-1410G>C
XR_938995.1:n.735-1410G>C
XR_001741765.1:n.2908-1410G>C
XR_001741766.1:n.1680-1410G>C
XR_938982.2:n.3490-1410G>C
XR_938984.2:n.2912-1410G>C
XR_938985.2:n.1944-1410G>C
XR_938986.2:n.581-1410G>C
XR_938987.2:n.870-1410G>C
XR_938989.2:n.354-1410G>C