Canonical Allele Identifier: CA190405459

Gene: BNC2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.16512750A>G , CM000671.2:g.16512750A>G	GRCh38
NC_000009.11:g.16512748A>G , CM000671.1:g.16512748A>G	GRCh37
NC_000009.10:g.16502748A>G	NCBI36
NG_051226.1:g.363089T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700553.1:c.339+39780T>C	ENSP00000515060.1:n.339+39780T>C
ENST00000380672.9:c.669+39780T>C MANE Select	ENSP00000370047.3:n.669+39780T>C
ENST00000380666.6:c.435+39780T>C	ENSP00000370041.3:n.435+39780T>C
ENST00000380667.6:c.468+39780T>C	ENSP00000370042.1:n.468+39780T>C
ENST00000380672.8:c.669+39780T>C	ENSP00000370047.3:n.669+39780T>C
ENST00000418777.5:c.540+39780T>C	ENSP00000408370.1:n.540+39780T>C
ENST00000484726.5:c.669+39780T>C	ENSP00000431516.1:n.669+39780T>C
ENST00000545497.5:c.147+39780T>C	ENSP00000444640.2:n.147+39780T>C
ENST00000603713.5:c.435+39780T>C	ENSP00000474045.1:n.435+39780T>C
NM_017637.5:c.669+39780T>C	NP_060107.3:n.669+39780T>C
XM_011517921.1:c.753+39780T>C	XP_011516223.1:n.753+39780T>C
XM_011517922.1:c.711+39780T>C	XP_011516224.1:n.711+39780T>C
XM_011517923.1:c.711+39780T>C	XP_011516225.1:n.711+39780T>C
XM_011517924.1:c.543+39780T>C	XP_011516226.1:n.543+39780T>C
XM_011517925.1:c.372+39780T>C	XP_011516227.1:n.372+39780T>C
XM_011517926.1:c.342+39780T>C	XP_011516228.1:n.342+39780T>C
XM_011517927.1:c.147+39780T>C	XP_011516229.1:n.147+39780T>C
XM_011517928.1:c.795+39780T>C	XP_011516230.1:n.795+39780T>C
XM_011517929.1:c.-37+33935T>C	XP_011516231.1:n.-37+33935T>C
XM_011517930.1:c.-37+35388T>C	XP_011516232.1:n.-37+35388T>C
XM_011517933.1:c.543+39780T>C	XP_011516235.1:n.543+39780T>C
XM_011517934.1:c.147+39780T>C	XP_011516236.1:n.147+39780T>C
NM_001317939.1:c.543+39780T>C	NP_001304868.1:n.543+39780T>C
NM_001317940.1:c.384+39780T>C	NP_001304869.1:n.384+39780T>C
XM_011517924.2:c.543+39780T>C	XP_011516226.1:n.543+39780T>C
XM_011517934.2:c.147+39780T>C	XP_011516236.1:n.147+39780T>C
XM_017014816.1:c.795+39780T>C	XP_016870305.1:n.795+39780T>C
XM_017014817.1:c.795+39780T>C	XP_016870306.1:n.795+39780T>C
XM_017014818.1:c.711+39780T>C	XP_016870307.1:n.711+39780T>C
XM_017014819.1:c.795+39780T>C	XP_016870308.1:n.795+39780T>C
XM_017014820.1:c.795+39780T>C	XP_016870309.1:n.795+39780T>C
XM_017014821.1:c.711+39780T>C	XP_016870310.1:n.711+39780T>C
XM_017014822.1:c.342+39780T>C	XP_016870311.1:n.342+39780T>C
XM_017014823.1:c.342+39780T>C	XP_016870312.1:n.342+39780T>C
XM_017014824.1:c.147+39780T>C	XP_016870313.1:n.147+39780T>C
XM_017014825.2:c.795+39780T>C	XP_016870314.1:n.795+39780T>C
XM_017014826.1:c.795+39780T>C	XP_016870315.1:n.795+39780T>C
XM_017014827.1:c.795+39780T>C	XP_016870316.1:n.795+39780T>C
XM_017014828.1:c.795+39780T>C	XP_016870317.1:n.795+39780T>C
XM_017014829.2:c.-37+35388T>C	XP_016870318.1:n.-37+35388T>C
NM_017637.6:c.669+39780T>C MANE Select	NP_060107.3:n.669+39780T>C
NM_001317939.2:c.543+39780T>C	NP_001304868.1:n.543+39780T>C
NM_001317940.2:c.384+39780T>C	NP_001304869.1:n.384+39780T>C