Canonical Allele Identifier: CA1610179956
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1780274528
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897363G>T , CM000668.2:g.10897363G>T GRCh38
NC_000006.11:g.10897596G>T , CM000668.1:g.10897596G>T GRCh37
NC_000006.10:g.11005582G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-648G>T MANE Select ENSP00000283141.6:n.337-648G>T
ENST00000283141.10:c.337-648G>T ENSP00000283141.6:n.337-648G>T
ENST00000341041.8:c.337-648G>T ENSP00000340320.4:n.337-648G>T
ENST00000480294.1:c.*299-648G>T ENSP00000417929.1:n.*299-648G>T
ENST00000543878.5:c.334-648G>T ENSP00000440676.2:n.334-648G>T
NM_001040274.2:c.337-648G>T NP_001035364.2:n.337-648G>T
NM_001040274.3:c.337-648G>T MANE Select NP_001035364.2:n.337-648G>T
Search 100 bp 5'
Search 100 bp 3'