Canonical Allele Identifier: CA13768589
Gene: BICDL1 HGNC NCBI

Linked Data

dbSNP Id: rs11064994

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120017960A>G , CM000674.2:g.120017960A>G GRCh38
NC_000012.11:g.120455764A>G , CM000674.1:g.120455764A>G GRCh37
NC_000012.10:g.118940147A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000548673.6:c.645+19224A>G MANE Select ENSP00000447477.2:n.645+19224A>G
ENST00000397558.6:c.645+19224A>G ENSP00000380690.2:n.645+19224A>G
ENST00000546420.5:c.786+18048A>G
NM_207311.2:c.645+19224A>G NP_997194.2:n.645+19224A>G
XM_005253991.3:c.645+19224A>G XP_005254048.1:n.645+19224A>G
XM_006719694.2:c.645+19224A>G XP_006719757.1:n.645+19224A>G
XM_006719696.2:c.645+19224A>G XP_006719759.1:n.645+19224A>G
XM_006719697.2:c.645+19224A>G XP_006719760.1:n.645+19224A>G
XM_011538999.1:c.645+19224A>G XP_011537301.1:n.645+19224A>G
XM_011539000.1:c.33+18048A>G XP_011537302.1:n.33+18048A>G
XR_944834.1:n.705+19224A>G
XR_944836.1:n.705+19224A>G
NR_147892.1:n.670+19224A>G
NR_147893.1:n.670+19224A>G
NR_147894.1:n.822+18048A>G
XM_005253991.4:c.645+19224A>G XP_005254048.1:n.645+19224A>G
XM_006719694.3:c.645+19224A>G XP_006719757.1:n.645+19224A>G
XM_006719696.3:c.645+19224A>G XP_006719759.1:n.645+19224A>G
XM_006719697.3:c.645+19224A>G XP_006719760.1:n.645+19224A>G
XM_011538999.2:c.645+19224A>G XP_011537301.1:n.645+19224A>G
XM_011539000.2:c.33+18048A>G XP_011537302.1:n.33+18048A>G
XR_001748923.1:n.698+19224A>G
XR_944834.2:n.699+19224A>G
XR_944836.3:n.699+19224A>G
NM_001367886.1:c.645+19224A>G MANE Select NP_001354815.1:n.645+19224A>G