Canonical Allele Identifier: CA11143069
Gene: BOK HGNC NCBI

Linked Data

dbSNP Id: rs12479254

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.241563541C>T , CM000664.2:g.241563541C>T GRCh38
NC_000002.11:g.242502956C>T , CM000664.1:g.242502956C>T GRCh37
NC_000002.10:g.242151629C>T NCBI36
NG_029488.1:g.9765C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000318407.5:c.349+1065C>T MANE Select ENSP00000314132.3:n.349+1065C>T
ENST00000318407.4:c.349+1065C>T ENSP00000314132.3:n.349+1065C>T
NM_032515.4:c.349+1065C>T NP_115904.1:n.349+1065C>T
XM_005247037.3:c.349+1065C>T XP_005247094.1:n.349+1065C>T
XM_005247039.3:c.115+1065C>T XP_005247096.1:n.115+1065C>T
XM_011511696.1:c.349+1065C>T XP_011509998.1:n.349+1065C>T
XM_011511697.1:c.349+1065C>T XP_011509999.1:n.349+1065C>T
XM_011511696.2:c.349+1065C>T XP_011509998.1:n.349+1065C>T
XM_011511697.3:c.349+1065C>T XP_011509999.1:n.349+1065C>T
XM_017004775.1:c.115+1065C>T XP_016860264.1:n.115+1065C>T
XM_017004776.1:c.115+1065C>T XP_016860265.1:n.115+1065C>T
NM_032515.5:c.349+1065C>T MANE Select NP_115904.1:n.349+1065C>T