Canonical Allele Identifier: CA817016281
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1267449769
gnomAD v3: 6-10921307-T-C
gnomAD v4: 6-10921307-T-C
MyVariant Identifiers: chr6:g.10921540T>C (hg19) chr6:g.10921307T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921307T>C , CM000668.2:g.10921307T>C GRCh38
NC_000006.11:g.10921540T>C , CM000668.1:g.10921540T>C GRCh37
NC_000006.10:g.11029526T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3189T>C MANE Select ENSP00000283141.6:n.1073-3189T>C
ENST00000283141.10:c.1073-3189T>C ENSP00000283141.6:n.1073-3189T>C
ENST00000341041.8:c.*151-1384T>C ENSP00000340320.4:n.*151-1384T>C
ENST00000480294.1:c.*1035-3189T>C ENSP00000417929.1:n.*1035-3189T>C
ENST00000487561.2:c.556-3189T>C ENSP00000417870.1:n.556-3189T>C
ENST00000543878.5:c.1070-3189T>C ENSP00000440676.2:n.1070-3189T>C
NM_001040274.2:c.1073-3189T>C NP_001035364.2:n.1073-3189T>C
NM_001040274.3:c.1073-3189T>C MANE Select NP_001035364.2:n.1073-3189T>C
Search 100 bp 5'
Search 100 bp 3'