Canonical Allele Identifier: CA565388177
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1471172074
gnomAD v2: 6-10897533-A-G
gnomAD v3: 6-10897300-A-G
gnomAD v4: 6-10897300-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897300A>G , CM000668.2:g.10897300A>G GRCh38
NC_000006.11:g.10897533A>G , CM000668.1:g.10897533A>G GRCh37
NC_000006.10:g.11005519A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-711A>G MANE Select ENSP00000283141.6:n.337-711A>G
ENST00000283141.10:c.337-711A>G ENSP00000283141.6:n.337-711A>G
ENST00000341041.8:c.337-711A>G ENSP00000340320.4:n.337-711A>G
ENST00000480294.1:c.*299-711A>G ENSP00000417929.1:n.*299-711A>G
ENST00000543878.5:c.334-711A>G ENSP00000440676.2:n.334-711A>G
NM_001040274.2:c.337-711A>G NP_001035364.2:n.337-711A>G
NM_001040274.3:c.337-711A>G MANE Select NP_001035364.2:n.337-711A>G