Canonical Allele Identifier: CA1955071943

Gene: NUCB2

Linked Data

• dbSNP Id: rs1941371026

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17276602T>C , CM000673.2:g.17276602T>C	GRCh38
NC_000011.9:g.17298149T>C , CM000673.1:g.17298149T>C	GRCh37
NC_000011.8:g.17254725T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000646648.1:c.-156+399T>C	ENSP00000495210.1:n.-156+399T>C
ENST00000526120.5:c.-155-6187T>C	ENSP00000436215.1:n.-155-6187T>C
ENST00000528644.5:c.-155-6187T>C	ENSP00000431136.1:n.-155-6187T>C
ENST00000530527.5:c.-362+399T>C	ENSP00000435160.1:n.-362+399T>C
ENST00000533773.5:c.-156+399T>C	ENSP00000433542.1:n.-156+399T>C
XM_011520120.1:c.-359+399T>C	XP_011518422.1:n.-359+399T>C
XM_011520126.1:c.-156+399T>C	XP_011518428.1:n.-156+399T>C
XM_011520127.1:c.-155-6187T>C	XP_011518429.1:n.-155-6187T>C
XM_011520129.1:c.-235-6187T>C	XP_011518431.1:n.-235-6187T>C
XM_011520131.1:c.-359+399T>C	XP_011518433.1:n.-359+399T>C
XM_011520132.1:c.-359+399T>C	XP_011518434.1:n.-359+399T>C
XM_011520133.1:c.-359+399T>C	XP_011518435.1:n.-359+399T>C
XM_017017815.1:c.-240+399T>C	XP_016873304.1:n.-240+399T>C
XM_024448537.1:c.-155-6187T>C	XP_024304305.1:n.-155-6187T>C
XM_024448543.1:c.-240+123T>C	XP_024304311.1:n.-240+123T>C
XM_024448544.1:c.-236+399T>C	XP_024304312.1:n.-236+399T>C
XM_024448546.1:c.-235-6187T>C	XP_024304314.1:n.-235-6187T>C