Canonical Allele Identifier: CA1836311741

Gene: BNC2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16795243T>G , CM000671.2:g.16795243T>G	GRCh38
NC_000009.11:g.16795241T>G , CM000671.1:g.16795241T>G	GRCh37
NC_000009.10:g.16785241T>G	NCBI36
NG_051226.1:g.80596A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380672.9:c.4-56758A>C MANE Select	ENSP00000370047.3:n.4-56758A>C
ENST00000380666.6:c.-105-67246A>C	ENSP00000370041.3:n.-105-67246A>C
ENST00000380667.6:c.4-56758A>C	ENSP00000370042.1:n.4-56758A>C
ENST00000380672.8:c.4-56758A>C	ENSP00000370047.3:n.4-56758A>C
ENST00000484726.5:c.4-56758A>C	ENSP00000431516.1:n.4-56758A>C
ENST00000486514.5:c.4-67246A>C	ENSP00000474647.1:n.4-67246A>C
ENST00000545497.5:c.-393-67246A>C	ENSP00000444640.2:n.-393-67246A>C
ENST00000613349.4:c.-105-67246A>C	ENSP00000477717.1:n.-105-67246A>C
ENST00000617779.1:c.-231-56758A>C	ENSP00000482793.1:n.-231-56758A>C
NM_017637.5:c.4-56758A>C	NP_060107.3:n.4-56758A>C
XM_011517921.1:c.4-56758A>C	XP_011516223.1:n.4-56758A>C
XM_011517922.1:c.45+37001A>C	XP_011516224.1:n.45+37001A>C
XM_011517923.1:c.45+37001A>C	XP_011516225.1:n.45+37001A>C
XM_011517924.1:c.4-67246A>C	XP_011516226.1:n.4-67246A>C
XM_011517926.1:c.3+75403A>C	XP_011516228.1:n.3+75403A>C
XM_011517928.1:c.45+37001A>C	XP_011516230.1:n.45+37001A>C
XM_011517933.1:c.4-67246A>C	XP_011516235.1:n.4-67246A>C
NM_001317939.1:c.4-67246A>C	NP_001304868.1:n.4-67246A>C
NM_001317940.1:c.45+37001A>C	NP_001304869.1:n.45+37001A>C
XM_011517924.2:c.4-67246A>C	XP_011516226.1:n.4-67246A>C
XM_017014816.1:c.45+37001A>C	XP_016870305.1:n.45+37001A>C
XM_017014817.1:c.45+37001A>C	XP_016870306.1:n.45+37001A>C
XM_017014818.1:c.45+37001A>C	XP_016870307.1:n.45+37001A>C
XM_017014819.1:c.45+37001A>C	XP_016870308.1:n.45+37001A>C
XM_017014820.1:c.45+37001A>C	XP_016870309.1:n.45+37001A>C
XM_017014821.1:c.45+37001A>C	XP_016870310.1:n.45+37001A>C
XM_017014825.2:c.45+37001A>C	XP_016870314.1:n.45+37001A>C
XM_017014826.1:c.45+37001A>C	XP_016870315.1:n.45+37001A>C
XM_017014827.1:c.45+37001A>C	XP_016870316.1:n.45+37001A>C
XM_017014828.1:c.45+37001A>C	XP_016870317.1:n.45+37001A>C
NM_017637.6:c.4-56758A>C MANE Select	NP_060107.3:n.4-56758A>C
NM_001317939.2:c.4-67246A>C	NP_001304868.1:n.4-67246A>C
NM_001317940.2:c.45+37001A>C	NP_001304869.1:n.45+37001A>C