Canonical Allele Identifier: CA101509425
Gene: SNCA HGNC NCBI
SNCA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1051138421
gnomAD v2: 4-90759070-A-T
gnomAD v3: 4-89837919-A-T
gnomAD v4: 4-89837919-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89837919A>T , CM000666.2:g.89837919A>T GRCh38
NC_000004.11:g.90759070A>T , CM000666.1:g.90759070A>T GRCh37
NC_000004.10:g.90978093A>T NCBI36
NG_011851.1:g.5378T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336904.7:c.-26+333T>A (SNCA) ENSP00000338345.3:n.-26+333T>A
NM_001146055.1:c.-26+333T>A (SNCA) NP_001139527.1:n.-26+333T>A
NR_045481.1:n.335-342A>T (SNCA-AS1)
XM_011532205.1:c.-26+333T>A (SNCA) XP_011530507.1:n.-26+333T>A
XM_011532205.2:c.-26+333T>A (SNCA) XP_011530507.1:n.-26+333T>A
NM_001146055.2:c.-26+333T>A (SNCA) NP_001139527.1:n.-26+333T>A
NM_001375285.1:c.-95+333T>A (SNCA) NP_001362214.1:n.-95+333T>A
NR_164674.1:n.53+333T>A (SNCA)