Canonical Allele Identifier: CA2302428766
Gene: MYO5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49878950T= , CM000680.2:g.49878950T= GRCh38
NC_000018.9:g.47405320T= , CM000680.1:g.47405320T= GRCh37
NC_000018.8:g.45659318T= NCBI36
NG_012925.1:g.321132A=
NG_012925.2:g.321132A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697218.1:n.25A=
ENST00000697219.1:c.3068A=
ENST00000285039.12:c.3271A= MANE Select ENSP00000285039.6:p.Ile1091=
ENST00000285039.11:c.3271A= ENSP00000285039.6:p.Ile1091=
ENST00000324581.10:c.700A= ENSP00000315531.7:p.Ile234=
ENST00000589568.1:n.472A=
ENST00000616031.4:c.1907-42217A= ENSP00000479038.1:n.1907-42217A=
NM_001080467.2:c.3271A= NP_001073936.1:p.Ile1091=
NM_001080467.3:c.3271A= MANE Select NP_001073936.1:p.Ile1091=