Canonical Allele Identifier: CA817022004
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1330997112
MyVariant Identifiers: chr6:g.10897549T>C (hg19) chr6:g.10897316T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897316T>C , CM000668.2:g.10897316T>C GRCh38
NC_000006.11:g.10897549T>C , CM000668.1:g.10897549T>C GRCh37
NC_000006.10:g.11005535T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-695T>C MANE Select ENSP00000283141.6:n.337-695T>C
ENST00000283141.10:c.337-695T>C ENSP00000283141.6:n.337-695T>C
ENST00000341041.8:c.337-695T>C ENSP00000340320.4:n.337-695T>C
ENST00000480294.1:c.*299-695T>C ENSP00000417929.1:n.*299-695T>C
ENST00000543878.5:c.334-695T>C ENSP00000440676.2:n.334-695T>C
NM_001040274.2:c.337-695T>C NP_001035364.2:n.337-695T>C
NM_001040274.3:c.337-695T>C MANE Select NP_001035364.2:n.337-695T>C
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