Canonical Allele Identifier: CA134131421
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1051304655
MyVariant Identifiers: chr6:g.10921579T>G (hg19) chr6:g.10921346T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921346T>G , CM000668.2:g.10921346T>G GRCh38
NC_000006.11:g.10921579T>G , CM000668.1:g.10921579T>G GRCh37
NC_000006.10:g.11029565T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3150T>G MANE Select ENSP00000283141.6:n.1073-3150T>G
ENST00000283141.10:c.1073-3150T>G ENSP00000283141.6:n.1073-3150T>G
ENST00000341041.8:c.*151-1345T>G ENSP00000340320.4:n.*151-1345T>G
ENST00000480294.1:c.*1035-3150T>G ENSP00000417929.1:n.*1035-3150T>G
ENST00000487561.2:c.556-3150T>G ENSP00000417870.1:n.556-3150T>G
ENST00000543878.5:c.1070-3150T>G ENSP00000440676.2:n.1070-3150T>G
NM_001040274.2:c.1073-3150T>G NP_001035364.2:n.1073-3150T>G
NM_001040274.3:c.1073-3150T>G MANE Select NP_001035364.2:n.1073-3150T>G
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