Canonical Allele Identifier: CA817021997
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs113058324
gnomAD v3: 6-10897287-A-C
gnomAD v4: 6-10897287-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897287A>C , CM000668.2:g.10897287A>C GRCh38
NC_000006.11:g.10897520A>C , CM000668.1:g.10897520A>C GRCh37
NC_000006.10:g.11005506A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-724A>C MANE Select ENSP00000283141.6:n.337-724A>C
ENST00000283141.10:c.337-724A>C ENSP00000283141.6:n.337-724A>C
ENST00000341041.8:c.337-724A>C ENSP00000340320.4:n.337-724A>C
ENST00000480294.1:c.*299-724A>C ENSP00000417929.1:n.*299-724A>C
ENST00000543878.5:c.334-724A>C ENSP00000440676.2:n.334-724A>C
NM_001040274.2:c.337-724A>C NP_001035364.2:n.337-724A>C
NM_001040274.3:c.337-724A>C MANE Select NP_001035364.2:n.337-724A>C