Canonical Allele Identifier: CA553251018

Gene: SNCA SNCA-AS1

Linked Data

• dbSNP Id: rs1203289494
• gnomAD v2: 4-90759118-T-A
• gnomAD v3: 4-89837967-T-A
• gnomAD v4: 4-89837967-T-A
• MyVariant Identifiers: chr4:g.90759118T>A (hg19) ; chr4:g.89837967T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89837967T>A , CM000666.2:g.89837967T>A	GRCh38
NC_000004.11:g.90759118T>A , CM000666.1:g.90759118T>A	GRCh37
NC_000004.10:g.90978141T>A	NCBI36
NG_011851.1:g.5330A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336904.7:c.-26+285A>T (SNCA)	ENSP00000338345.3:n.-26+285A>T
NM_001146055.1:c.-26+285A>T (SNCA)	NP_001139527.1:n.-26+285A>T
NR_045481.1:n.335-294T>A (SNCA-AS1)
XM_011532205.1:c.-26+285A>T (SNCA)	XP_011530507.1:n.-26+285A>T
XM_011532205.2:c.-26+285A>T (SNCA)	XP_011530507.1:n.-26+285A>T
NM_001146055.2:c.-26+285A>T (SNCA)	NP_001139527.1:n.-26+285A>T
NM_001375285.1:c.-95+285A>T (SNCA)	NP_001362214.1:n.-95+285A>T
NR_164674.1:n.53+285A>T (SNCA)