Canonical Allele Identifier: CA490290391
Gene: BLOC1S6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.45895310T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45603112T>G , CM000677.2:g.45603112T>G GRCh38
NC_000015.9:g.45895310T>G , CM000677.1:g.45895310T>G GRCh37
NC_000015.8:g.43682602T>G NCBI36
NG_028194.2:g.20894T>G , LRG_883:g.20894T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000220531.9:c.237T>G MANE Select ENSP00000220531.4:p.Val79=
ENST00000564310.2:c.166T>G
ENST00000565323.6:c.252T>G ENSP00000456851.1:p.Val84=
ENST00000672455.1:c.*230T>G ENSP00000500302.1:n.*230T>G
ENST00000220531.7:c.237T>G ENSP00000220531.3:p.Val79=
ENST00000562384.5:c.-55T>G ENSP00000457077.1:n.-55T>G
ENST00000563000.5:n.238-2316T>G
ENST00000563160.5:n.194-2316T>G
ENST00000564080.1:c.-18+15587T>G ENSP00000455047.1:n.-18+15587T>G
ENST00000564310.1:c.162T>G
ENST00000564765.1:c.-55T>G ENSP00000454537.1:n.-55T>G
ENST00000565216.5:c.114T>G ENSP00000456067.1:p.Val38=
ENST00000565323.5:c.252T>G ENSP00000456851.1:p.Val84=
ENST00000565409.5:c.-55T>G ENSP00000455599.1:n.-55T>G
ENST00000565727.5:n.106-2316T>G
ENST00000566184.1:n.148-2316T>G
ENST00000566801.5:c.-55T>G ENSP00000454715.1:n.-55T>G
ENST00000567461.5:c.-55T>G ENSP00000456152.1:n.-55T>G
ENST00000567523.5:c.233T>G ENSP00000456624.1:p.Leu78Trp
ENST00000567740.5:n.313-2316T>G
ENST00000568597.5:c.225-2316T>G ENSP00000454638.1:n.225-2316T>G
ENST00000568816.5:c.-55T>G ENSP00000455021.1:n.-55T>G
ENST00000568963.5:c.91T>G ENSP00000454438.1:p.Cys31Gly
ENST00000569076.5:c.87T>G ENSP00000454803.1:p.Val29=
NM_001311255.1:c.252T>G NP_001298184.1:p.Val84=
NM_001311256.1:c.240-2316T>G NP_001298185.1:n.240-2316T>G
NM_012388.2:c.237T>G NP_036520.1:p.Val79=
NM_012388.3:c.237T>G , LRG_883t1:c.237T>G NP_036520.1:p.Val79=
NR_132350.1:n.566T>G
NR_132351.1:n.554T>G
NR_132352.1:n.546-2316T>G
NR_132353.1:n.416T>G
NR_132354.1:n.412T>G
NR_132355.1:n.404-2316T>G
NR_132356.1:n.260T>G
NR_132357.1:n.260T>G
NR_132358.1:n.238-2316T>G
NR_132359.1:n.106-2316T>G
NM_012388.4:c.237T>G MANE Select NP_036520.1:p.Val79=
NR_132351.2:n.298T>G
NR_132352.2:n.290-2316T>G
NR_132355.2:n.148-2316T>G
NR_132356.2:n.260T>G
NR_132357.2:n.260T>G
NR_132359.2:n.106-2316T>G