Canonical Allele Identifier: CA190707171
Gene: BNC2 HGNC NCBI

Linked Data

dbSNP Id: rs10756819
gnomAD v3: 9-16858086-G-T
gnomAD v4: 9-16858086-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.16858086G>T , CM000671.2:g.16858086G>T GRCh38
NC_000009.11:g.16858084G>T , CM000671.1:g.16858084G>T GRCh37
NC_000009.10:g.16848084G>T NCBI36
NG_051226.1:g.17753C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380672.9:c.3+12560C>A MANE Select ENSP00000370047.3:n.3+12560C>A
ENST00000380666.6:c.-106+9863C>A ENSP00000370041.3:n.-106+9863C>A
ENST00000380667.6:c.3+12560C>A ENSP00000370042.1:n.3+12560C>A
ENST00000380672.8:c.3+12560C>A ENSP00000370047.3:n.3+12560C>A
ENST00000484726.5:c.3+12560C>A ENSP00000431516.1:n.3+12560C>A
ENST00000486514.5:c.3+12560C>A ENSP00000474647.1:n.3+12560C>A
ENST00000545497.5:c.-394+12560C>A ENSP00000444640.2:n.-394+12560C>A
ENST00000613349.4:c.-106+9273C>A ENSP00000477717.1:n.-106+9273C>A
ENST00000617779.1:c.-232+9273C>A ENSP00000482793.1:n.-232+9273C>A
NM_017637.5:c.3+12560C>A NP_060107.3:n.3+12560C>A
XM_011517921.1:c.3+12560C>A XP_011516223.1:n.3+12560C>A
XM_011517922.1:c.-63+12560C>A XP_011516224.1:n.-63+12560C>A
XM_011517923.1:c.-63+12560C>A XP_011516225.1:n.-63+12560C>A
XM_011517924.1:c.3+12560C>A XP_011516226.1:n.3+12560C>A
XM_011517926.1:c.3+12560C>A XP_011516228.1:n.3+12560C>A
XM_011517928.1:c.-63+12560C>A XP_011516230.1:n.-63+12560C>A
XM_011517933.1:c.3+12560C>A XP_011516235.1:n.3+12560C>A
NM_001317939.1:c.3+12560C>A NP_001304868.1:n.3+12560C>A
NM_001317940.1:c.-63+12560C>A NP_001304869.1:n.-63+12560C>A
XM_011517924.2:c.3+12560C>A XP_011516226.1:n.3+12560C>A
NM_017637.6:c.3+12560C>A MANE Select NP_060107.3:n.3+12560C>A
NM_001317939.2:c.3+12560C>A NP_001304868.1:n.3+12560C>A
NM_001317940.2:c.-63+12560C>A NP_001304869.1:n.-63+12560C>A