Canonical Allele Identifier: CA2427976076
Gene: SYN1 HGNC NCBI

Linked Data

dbSNP Id: rs2057834915
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47588424T>A , CM000685.2:g.47588424T>A GRCh38
NC_000023.10:g.47447823T>A , CM000685.1:g.47447823T>A GRCh37
NC_000023.9:g.47332767T>A NCBI36
NG_008437.1:g.36434A>T
NG_012533.1:g.11134T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.775-10923A>T MANE Select ENSP00000295987.7:n.775-10923A>T
ENST00000340666.5:c.775-10923A>T ENSP00000343206.4:n.775-10923A>T
ENST00000295987.11:c.775-10923A>T ENSP00000295987.7:n.775-10923A>T
ENST00000340666.4:c.775-10923A>T ENSP00000343206.4:n.775-10923A>T
NM_006950.3:c.775-10923A>T MANE Select NP_008881.2:n.775-10923A>T
NM_133499.2:c.775-10923A>T NP_598006.1:n.775-10923A>T
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