Canonical Allele Identifier: CA101496046

Gene: SNCA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89713869T>C , CM000666.2:g.89713869T>C	GRCh38
NC_000004.11:g.90635020T>C , CM000666.1:g.90635020T>C	GRCh37
NC_000004.10:g.90854043T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673902.1:c.391-11485A>G	ENSP00000501102.1:n.391-11485A>G
XR_938982.1:n.3490-5957T>C
XR_938984.1:n.2890-5957T>C
XR_938985.1:n.1922-5957T>C
XR_938986.1:n.556-5957T>C
XR_938987.1:n.810-5957T>C
XR_938988.1:n.676-5957T>C
XR_938989.1:n.332-5957T>C
XR_938990.1:n.420-5957T>C
XR_938991.1:n.435-5957T>C
XR_938993.1:n.437-5957T>C
XR_938994.1:n.901-5957T>C
XR_938995.1:n.735-5957T>C
XR_001741765.1:n.2908-5957T>C
XR_001741766.1:n.1680-5957T>C
XR_938982.2:n.3490-5957T>C
XR_938984.2:n.2912-5957T>C
XR_938985.2:n.1944-5957T>C
XR_938986.2:n.581-5957T>C
XR_938987.2:n.870-5957T>C
XR_938989.2:n.354-5957T>C