Canonical Allele Identifier: CA101509421

Gene: SNCA SNCA-AS1

Linked Data

• dbSNP Id: rs1054188897
• gnomAD v2: 4-90758994-C-T
• gnomAD v3: 4-89837843-C-T
• gnomAD v4: 4-89837843-C-T
• MyVariant Identifiers: chr4:g.90758994C>T (hg19) ; chr4:g.89837843C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89837843C>T , CM000666.2:g.89837843C>T	GRCh38
NC_000004.11:g.90758994C>T , CM000666.1:g.90758994C>T	GRCh37
NC_000004.10:g.90978017C>T	NCBI36
NG_011851.1:g.5454G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336904.7:c.-26+409G>A (SNCA)	ENSP00000338345.3:n.-26+409G>A
NM_001146055.1:c.-26+409G>A (SNCA)	NP_001139527.1:n.-26+409G>A
NR_045481.1:n.335-418C>T (SNCA-AS1)
XM_011532205.1:c.-26+409G>A (SNCA)	XP_011530507.1:n.-26+409G>A
XM_011532205.2:c.-26+409G>A (SNCA)	XP_011530507.1:n.-26+409G>A
NM_001146055.2:c.-26+409G>A (SNCA)	NP_001139527.1:n.-26+409G>A
NM_001375285.1:c.-95+409G>A (SNCA)	NP_001362214.1:n.-95+409G>A
NR_164674.1:n.53+409G>A (SNCA)