Canonical Allele Identifier: CA1890225064
Gene: CELF2 HGNC NCBI

Linked Data

dbSNP Id: rs1589061308

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.10560256A>T , CM000672.2:g.10560256A>T GRCh38
NC_000010.10:g.10602219A>T , CM000672.1:g.10602219A>T GRCh37
NC_000010.9:g.10642225A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001326317.1:c.-95+97670A>T NP_001313246.1:n.-95+97670A>T
NM_001326318.1:c.-95+97670A>T NP_001313247.1:n.-95+97670A>T
NM_001326319.1:c.-133+97670A>T NP_001313248.1:n.-133+97670A>T
NM_001326320.1:c.-189+97670A>T NP_001313249.1:n.-189+97670A>T
NM_001326321.1:c.-95+97670A>T NP_001313250.1:n.-95+97670A>T
NM_001326323.1:c.-189+97670A>T NP_001313252.1:n.-189+97670A>T
XM_017015557.1:c.-273+97670A>T XP_016871046.1:n.-273+97670A>T
XM_017015568.2:c.-627+97670A>T XP_016871057.1:n.-627+97670A>T
NM_001326317.2:c.-95+97670A>T NP_001313246.1:n.-95+97670A>T
NM_001326318.2:c.-95+97670A>T NP_001313247.1:n.-95+97670A>T
NM_001326319.2:c.-133+97670A>T NP_001313248.1:n.-133+97670A>T
NM_001326320.2:c.-189+97670A>T NP_001313249.1:n.-189+97670A>T
NM_001326321.2:c.-95+97670A>T NP_001313250.1:n.-95+97670A>T
NM_001326323.2:c.-189+97670A>T NP_001313252.1:n.-189+97670A>T