Canonical Allele Identifier: CA875829609
Gene: SYN1 HGNC NCBI

Linked Data

dbSNP Id: rs1180984758
MyVariant Identifiers: chrX:g.47447990C>A (hg19) chrX:g.47588591C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47588591C>A , CM000685.2:g.47588591C>A GRCh38
NC_000023.10:g.47447990C>A , CM000685.1:g.47447990C>A GRCh37
NC_000023.9:g.47332934C>A NCBI36
NG_008437.1:g.36267G>T
NG_012533.1:g.11301C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.775-11090G>T MANE Select ENSP00000295987.7:n.775-11090G>T
ENST00000340666.5:c.775-11090G>T ENSP00000343206.4:n.775-11090G>T
ENST00000295987.11:c.775-11090G>T ENSP00000295987.7:n.775-11090G>T
ENST00000340666.4:c.775-11090G>T ENSP00000343206.4:n.775-11090G>T
NM_006950.3:c.775-11090G>T MANE Select NP_008881.2:n.775-11090G>T
NM_133499.2:c.775-11090G>T NP_598006.1:n.775-11090G>T
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