Canonical Allele Identifier: CA1610179600
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1780270638

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897113A>T , CM000668.2:g.10897113A>T GRCh38
NC_000006.11:g.10897346A>T , CM000668.1:g.10897346A>T GRCh37
NC_000006.10:g.11005332A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-898A>T MANE Select ENSP00000283141.6:n.337-898A>T
ENST00000283141.10:c.337-898A>T ENSP00000283141.6:n.337-898A>T
ENST00000341041.8:c.337-898A>T ENSP00000340320.4:n.337-898A>T
ENST00000480294.1:c.*299-898A>T ENSP00000417929.1:n.*299-898A>T
ENST00000543878.5:c.334-898A>T ENSP00000440676.2:n.334-898A>T
NM_001040274.2:c.337-898A>T NP_001035364.2:n.337-898A>T
NM_001040274.3:c.337-898A>T MANE Select NP_001035364.2:n.337-898A>T