Canonical Allele Identifier: CA15688793
Gene: NUCB2 HGNC NCBI

Linked Data

dbSNP Id: rs214101

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17267807A>G , CM000673.2:g.17267807A>G GRCh38
NC_000011.9:g.17289354A>G , CM000673.1:g.17289354A>G GRCh37
NC_000011.8:g.17245930A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000646648.1:c.-498-1378A>G ENSP00000495210.1:n.-498-1378A>G
ENST00000528644.5:c.-155-14982A>G ENSP00000431136.1:n.-155-14982A>G
ENST00000530527.5:c.-1002+126A>G ENSP00000435160.1:n.-1002+126A>G
ENST00000620945.1:n.930-261A>G
XM_011520126.1:c.-498-1378A>G XP_011518428.1:n.-498-1378A>G
XM_011520127.1:c.-302-1378A>G XP_011518429.1:n.-302-1378A>G
XM_011520129.1:c.-382-1378A>G XP_011518431.1:n.-382-1378A>G
XM_017017815.1:c.-582-1378A>G XP_016873304.1:n.-582-1378A>G
XM_024448537.1:c.-302-1378A>G XP_024304305.1:n.-302-1378A>G
XM_024448544.1:c.-578-1378A>G XP_024304312.1:n.-578-1378A>G
XM_024448546.1:c.-382-1378A>G XP_024304314.1:n.-382-1378A>G