Canonical Allele Identifier: CA1085947920

Gene: SYCP2L

Linked Data

• dbSNP Id: rs1780269756
• gnomAD v3: 6-10897061-G-C
• gnomAD v4: 6-10897061-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897061G>C , CM000668.2:g.10897061G>C	GRCh38
NC_000006.11:g.10897294G>C , CM000668.1:g.10897294G>C	GRCh37
NC_000006.10:g.11005280G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000283141.11:c.337-950G>C MANE Select	ENSP00000283141.6:n.337-950G>C
ENST00000283141.10:c.337-950G>C	ENSP00000283141.6:n.337-950G>C
ENST00000341041.8:c.337-950G>C	ENSP00000340320.4:n.337-950G>C
ENST00000480294.1:c.*299-950G>C	ENSP00000417929.1:n.*299-950G>C
ENST00000543878.5:c.334-950G>C	ENSP00000440676.2:n.334-950G>C
NM_001040274.2:c.337-950G>C	NP_001035364.2:n.337-950G>C
NM_001040274.3:c.337-950G>C MANE Select	NP_001035364.2:n.337-950G>C