Canonical Allele Identifier: CA12357525
Gene: L3MBTL3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1415701

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.130024690G>A , CM000668.2:g.130024690G>A GRCh38
NC_000006.11:g.130345835G>A , CM000668.1:g.130345835G>A GRCh37
NC_000006.10:g.130387528G>A NCBI36
NG_051942.1:g.11322G>A

Transcript Alleles

HGVS Amino-acid change
NM_001007102.2:c.-16+2385G>A VV NP_001007103.1:p.=
NM_032438.2:c.-16+2385G>A VV NP_115814.1:p.=
XM_005267161.3:c.-16+2385G>A XP_005267218.1:p.=
XM_006715576.2:c.-16+2385G>A XP_006715639.1:p.=
XM_006715578.2:c.-16+2385G>A XP_006715641.1:p.=
XM_011536179.1:c.-16+2385G>A XP_011534481.1:p.=
XM_011536180.1:c.-16+2385G>A XP_011534482.1:p.=
XM_011536181.1:c.-16+2385G>A XP_011534483.1:p.=
XM_011536182.1:c.-16+2385G>A XP_011534484.1:p.=
XM_011536183.1:c.-16+2385G>A XP_011534485.1:p.=
XM_011536184.1:c.-16+2385G>A XP_011534486.1:p.=
NM_001007102.3:c.-16+2385G>A VV NP_001007103.1:p.=
NM_001346550.1:c.-16+2385G>A VV NP_001333479.1:p.=
NM_001346551.1:c.-16+2385G>A VV NP_001333480.1:p.=
NM_032438.3:c.-16+2385G>A VV NP_115814.1:p.=
XM_005267161.4:c.-16+2385G>A XP_005267218.1:p.=
XM_006715576.3:c.-16+2385G>A XP_006715639.1:p.=
XM_006715578.3:c.-16+2385G>A XP_006715641.1:p.=
XM_011536179.3:c.-16+2385G>A XP_011534481.1:p.=
XM_011536180.2:c.-16+2385G>A XP_011534482.1:p.=
XM_011536181.2:c.-16+2385G>A XP_011534483.1:p.=
XM_011536183.2:c.-16+2385G>A XP_011534485.1:p.=
XM_011536184.2:c.-16+2385G>A XP_011534486.1:p.=
ENST00000361794.6:c.-16+2385G>A ENSP00000354526.2:p.=
ENST00000368136.2:c.-16+2385G>A ENSP00000357118.2:p.=
ENST00000368139.6:c.-16+4022G>A ENSP00000357121.2:p.=
ENST00000526019.5:c.-16+2385G>A ENSP00000436706.1:p.=
ENST00000526087.5:c.-16+2385G>A ENSP00000436617.1:p.=
ENST00000528385.5:c.-16+2385G>A ENSP00000433257.1:p.=
ENST00000529410.5:c.-16+2385G>A ENSP00000431962.1:p.=
ENST00000533560.5:c.-16+2385G>A ENSP00000437185.1:p.=