Canonical Allele Identifier: CA1188121099
Gene: SYPL2 HGNC NCBI

Linked Data

dbSNP Id: rs1656140975
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109480846C>T , CM000663.2:g.109480846C>T GRCh38
NC_000001.10:g.110023468C>T , CM000663.1:g.110023468C>T GRCh37
NC_000001.9:g.109824991C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369872.4:c.*1298C>T MANE Select ENSP00000358888.3:n.*1298C>T
ENST00000369872.3:c.*1298C>T ENSP00000358888.3:n.*1298C>T
NM_001040709.1:c.*1298C>T NP_001035799.1:n.*1298C>T
XM_011541285.1:c.*1298C>T XP_011539587.1:n.*1298C>T
NM_001040709.2:c.*1298C>T MANE Select NP_001035799.1:n.*1298C>T
Search 100 bp 5'
Search 100 bp 3'