Canonical Allele Identifier: CA1881299005

Gene: FUBP3

Linked Data

• dbSNP Id: rs7466269

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130588697A>C , CM000671.2:g.130588697A>C	GRCh38
NC_000009.11:g.133464084A>C , CM000671.1:g.133464084A>C	GRCh37
NC_000009.10:g.132453905A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699747.1:c.85-6786A>C	ENSP00000514557.1:n.85-6786A>C
ENST00000319725.10:c.85-6786A>C MANE Select	ENSP00000318177.9:n.85-6786A>C
ENST00000650723.1:c.*805-6786A>C	ENSP00000499109.1:n.*805-6786A>C
ENST00000319725.9:c.85-6786A>C	ENSP00000318177.9:n.85-6786A>C
ENST00000465949.1:n.420-6786A>C
NM_003934.1:c.85-6786A>C	NP_003925.1:n.85-6786A>C
XM_005272232.1:c.85-6786A>C	XP_005272289.1:n.85-6786A>C
XM_006717312.1:c.85-6786A>C	XP_006717375.1:n.85-6786A>C
XM_006717313.1:c.-177-6786A>C	XP_006717376.1:n.-177-6786A>C
XM_011519171.1:c.85-6786A>C	XP_011517473.1:n.85-6786A>C
XM_011519172.1:c.85-6786A>C	XP_011517474.1:n.85-6786A>C
XM_011519174.1:c.-422-4946A>C	XP_011517476.1:n.-422-4946A>C
XR_929871.1:n.199-6786A>C
XM_005272232.2:c.85-6786A>C	XP_005272289.1:n.85-6786A>C
XM_006717313.2:c.-177-6786A>C	XP_006717376.1:n.-177-6786A>C
XM_011519172.3:c.85-6786A>C	XP_011517474.1:n.85-6786A>C
XM_011519174.2:c.-422-4946A>C	XP_011517476.1:n.-422-4946A>C
XM_017015269.1:c.-177-6786A>C	XP_016870758.1:n.-177-6786A>C
XM_017015270.1:c.-443-6786A>C	XP_016870759.1:n.-443-6786A>C
XM_017015271.1:c.-688-4946A>C	XP_016870760.1:n.-688-4946A>C
XM_017015272.1:c.-338+8933A>C	XP_016870761.1:n.-338+8933A>C
XM_017015273.1:c.-443-6786A>C	XP_016870762.1:n.-443-6786A>C
XR_001746411.2:n.131-6786A>C
XR_001746412.2:n.131-6786A>C
NM_003934.2:c.85-6786A>C MANE Select	NP_003925.1:n.85-6786A>C