Canonical Allele Identifier: CA11653212

Gene: SNCA SNCA-AS1

Linked Data

• dbSNP Id: rs2619363
• gnomAD v2: 4-90759047-G-T
• gnomAD v3: 4-89837896-G-T
• gnomAD v4: 4-89837896-G-T
• MyVariant Identifiers: chr4:g.90759047G>T (hg19) ; chr4:g.89837896G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89837896G>T , CM000666.2:g.89837896G>T	GRCh38
NC_000004.11:g.90759047G>T , CM000666.1:g.90759047G>T	GRCh37
NC_000004.10:g.90978070G>T	NCBI36
NG_011851.1:g.5401C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336904.7:c.-26+356C>A (SNCA)	ENSP00000338345.3:n.-26+356C>A
NM_001146055.1:c.-26+356C>A (SNCA)	NP_001139527.1:n.-26+356C>A
NR_045481.1:n.335-365G>T (SNCA-AS1)
XM_011532205.1:c.-26+356C>A (SNCA)	XP_011530507.1:n.-26+356C>A
XM_011532205.2:c.-26+356C>A (SNCA)	XP_011530507.1:n.-26+356C>A
NM_001146055.2:c.-26+356C>A (SNCA)	NP_001139527.1:n.-26+356C>A
NM_001375285.1:c.-95+356C>A (SNCA)	NP_001362214.1:n.-95+356C>A
NR_164674.1:n.53+356C>A (SNCA)