Canonical Allele Identifier: CA1610179718
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1780271959

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897226A>G , CM000668.2:g.10897226A>G GRCh38
NC_000006.11:g.10897459A>G , CM000668.1:g.10897459A>G GRCh37
NC_000006.10:g.11005445A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-785A>G MANE Select ENSP00000283141.6:n.337-785A>G
ENST00000283141.10:c.337-785A>G ENSP00000283141.6:n.337-785A>G
ENST00000341041.8:c.337-785A>G ENSP00000340320.4:n.337-785A>G
ENST00000480294.1:c.*299-785A>G ENSP00000417929.1:n.*299-785A>G
ENST00000543878.5:c.334-785A>G ENSP00000440676.2:n.334-785A>G
NM_001040274.2:c.337-785A>G NP_001035364.2:n.337-785A>G
NM_001040274.3:c.337-785A>G MANE Select NP_001035364.2:n.337-785A>G