Canonical Allele Identifier: CA11134769
Gene: BOLL HGNC NCBI

Linked Data

dbSNP Id: rs700651

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.197766990G>A , CM000664.2:g.197766990G>A GRCh38
NC_000002.11:g.198631714G>A , CM000664.1:g.198631714G>A GRCh37
NC_000002.10:g.198339959G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696103.1:c.685-387C>T ENSP00000512398.1:n.685-387C>T
ENST00000392296.9:c.481-387C>T MANE Select ENSP00000376116.4:n.481-387C>T
ENST00000282278.12:c.154-387C>T ENSP00000282278.8:n.154-387C>T
ENST00000321801.11:c.517-387C>T ENSP00000314792.7:n.517-387C>T
ENST00000392296.8:c.481-387C>T ENSP00000376116.4:n.481-387C>T
ENST00000430004.5:c.481-387C>T ENSP00000397711.1:n.481-387C>T
ENST00000433157.1:c.481-387C>T ENSP00000396099.1:n.481-387C>T
ENST00000434976.5:c.*122-387C>T ENSP00000416911.1:n.*122-387C>T
NM_001284358.1:c.154-387C>T NP_001271287.1:n.154-387C>T
NM_001284361.1:c.499-387C>T NP_001271290.1:n.499-387C>T
NM_001284362.1:c.499-387C>T NP_001271291.1:n.499-387C>T
NM_033030.5:c.481-387C>T NP_149019.1:n.481-387C>T
NM_197970.2:c.517-387C>T NP_932074.1:n.517-387C>T
XM_006712715.2:c.517-387C>T XP_006712778.1:n.517-387C>T
XM_011511692.1:c.517-387C>T XP_011509994.1:n.517-387C>T
XM_011511693.1:c.517-387C>T XP_011509995.1:n.517-387C>T
XM_011511694.1:c.481-387C>T XP_011509996.1:n.481-387C>T
XM_011511695.1:c.517-387C>T XP_011509997.1:n.517-387C>T
XM_006712715.4:c.517-387C>T XP_006712778.1:n.517-387C>T
XM_011511692.3:c.517-387C>T XP_011509994.1:n.517-387C>T
XM_011511693.3:c.517-387C>T XP_011509995.1:n.517-387C>T
XM_011511694.2:c.481-387C>T XP_011509996.1:n.481-387C>T
XM_017004773.2:c.517-387C>T XP_016860262.1:n.517-387C>T
XM_024453053.1:c.511-387C>T XP_024308821.1:n.511-387C>T
XM_024453054.1:c.481-387C>T XP_024308822.1:n.481-387C>T
NM_001284361.2:c.499-387C>T NP_001271290.1:n.499-387C>T
NM_001284362.2:c.499-387C>T NP_001271291.1:n.499-387C>T
NM_033030.6:c.481-387C>T MANE Select NP_149019.1:n.481-387C>T
NM_197970.3:c.517-387C>T NP_932074.1:n.517-387C>T
NM_001284358.2:c.154-387C>T NP_001271287.1:n.154-387C>T