Canonical Allele Identifier: CA11653174
Gene: SNCA HGNC NCBI

Linked Data

dbSNP Id: rs356221
gnomAD v2: 4-90642464-A-T
gnomAD v3: 4-89721313-A-T
gnomAD v4: 4-89721313-A-T
MyVariant Identifiers: chr4:g.90642464A>T (hg19) chr4:g.89721313A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89721313A>T , CM000666.2:g.89721313A>T GRCh38
NC_000004.11:g.90642464A>T , CM000666.1:g.90642464A>T GRCh37
NC_000004.10:g.90861487A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000673902.1:c.390+7881T>A ENSP00000501102.1:n.390+7881T>A
XR_001741765.1:n.4196A>T
XR_001741766.1:n.2968A>T
XR_938982.2:n.4778A>T
XR_938984.2:n.4200A>T
XR_938985.2:n.3232A>T
XR_938986.2:n.1869A>T
XR_938987.2:n.2158A>T
XR_938989.2:n.1642A>T
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