Canonical Allele Identifier: CA2581700601
Gene: SYPL2 HGNC NCBI

Linked Data

gnomAD v4: 1-109480810-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109480810G>T , CM000663.2:g.109480810G>T GRCh38
NC_000001.10:g.110023432G>T , CM000663.1:g.110023432G>T GRCh37
NC_000001.9:g.109824955G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369872.4:c.*1262G>T MANE Select ENSP00000358888.3:n.*1262G>T
ENST00000369872.3:c.*1262G>T ENSP00000358888.3:n.*1262G>T
NM_001040709.1:c.*1262G>T NP_001035799.1:n.*1262G>T
XM_011541285.1:c.*1262G>T XP_011539587.1:n.*1262G>T
NM_001040709.2:c.*1262G>T MANE Select NP_001035799.1:n.*1262G>T
Search 100 bp 5'
Search 100 bp 3'