Canonical Allele Identifier: CA760578822
Gene: MYO3B HGNC NCBI

Linked Data

dbSNP Id: rs6749331

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.170604622T>A , CM000664.2:g.170604622T>A GRCh38
NC_000002.11:g.171461132T>A , CM000664.1:g.171461132T>A GRCh37
NC_000002.10:g.171169378T>A NCBI36
NG_034020.1:g.431478T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000408978.9:c.3734-47006T>A MANE Select ENSP00000386213.4:n.3734-47006T>A
ENST00000317935.10:c.3653-42287T>A ENSP00000314650.6:n.3653-42287T>A
ENST00000408978.8:c.3734-47006T>A ENSP00000386213.4:n.3734-47006T>A
ENST00000409044.7:c.3653-47006T>A ENSP00000386497.3:n.3653-47006T>A
ENST00000438642.6:n.3999-47006T>A
ENST00000602629.1:n.2962-47006T>A
NM_001083615.3:c.3653-47006T>A NP_001077084.2:n.3653-47006T>A
NM_138995.4:c.3734-47006T>A NP_620482.3:n.3734-47006T>A
NR_045682.1:n.3999-47006T>A
NR_045683.1:n.3877-42287T>A
NR_045684.1:n.3796-42287T>A
XM_006712299.2:c.3761-47006T>A XP_006712362.1:n.3761-47006T>A
XM_011510654.1:c.3869-47006T>A XP_011508956.1:n.3869-47006T>A
XM_011510655.1:c.3680-47006T>A XP_011508957.1:n.3680-47006T>A
XM_011510656.1:c.3176-47006T>A XP_011508958.1:n.3176-47006T>A
XM_011510657.1:c.2861-47006T>A XP_011508959.1:n.2861-47006T>A
XM_011510658.1:c.2861-47006T>A XP_011508960.1:n.2861-47006T>A
XM_006712299.4:c.3761-47006T>A XP_006712362.1:n.3761-47006T>A
XM_011510654.3:c.3869-47006T>A XP_011508956.1:n.3869-47006T>A
XM_011510655.3:c.3680-47006T>A XP_011508957.1:n.3680-47006T>A
XM_011510656.3:c.3176-47006T>A XP_011508958.1:n.3176-47006T>A
XM_011510657.3:c.2861-47006T>A XP_011508959.1:n.2861-47006T>A
XM_011510658.3:c.2861-47006T>A XP_011508960.1:n.2861-47006T>A
XM_024452713.1:c.2861-47006T>A XP_024308481.1:n.2861-47006T>A
NM_001083615.4:c.3653-47006T>A NP_001077084.2:n.3653-47006T>A
NM_138995.5:c.3734-47006T>A MANE Select NP_620482.3:n.3734-47006T>A
NR_045682.2:n.3997-47006T>A
NR_045683.2:n.3875-42287T>A
NR_045684.2:n.3794-42287T>A