Canonical Allele Identifier: CA2646937028
Gene: SYPL2 HGNC NCBI

Linked Data

gnomAD v4: 1-109480826-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109480826T>C , CM000663.2:g.109480826T>C GRCh38
NC_000001.10:g.110023448T>C , CM000663.1:g.110023448T>C GRCh37
NC_000001.9:g.109824971T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369872.4:c.*1278T>C MANE Select ENSP00000358888.3:n.*1278T>C
ENST00000369872.3:c.*1278T>C ENSP00000358888.3:n.*1278T>C
NM_001040709.1:c.*1278T>C NP_001035799.1:n.*1278T>C
XM_011541285.1:c.*1278T>C XP_011539587.1:n.*1278T>C
NM_001040709.2:c.*1278T>C MANE Select NP_001035799.1:n.*1278T>C
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