Canonical Allele Identifier: CA2302428763
Gene: MYO5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49878944C= , CM000680.2:g.49878944C= GRCh38
NC_000018.9:g.47405314C= , CM000680.1:g.47405314C= GRCh37
NC_000018.8:g.45659312C= NCBI36
NG_012925.1:g.321138G=
NG_012925.2:g.321138G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697218.1:n.31G=
ENST00000697219.1:c.3073+1G=
ENST00000285039.12:c.3276+1G= MANE Select ENSP00000285039.6:n.3276+1G=
ENST00000285039.11:c.3276+1G= ENSP00000285039.6:n.3276+1G=
ENST00000324581.10:c.705+1G= ENSP00000315531.7:n.705+1G=
ENST00000589568.1:n.477+1G=
ENST00000616031.4:c.1907-42211G= ENSP00000479038.1:n.1907-42211G=
NM_001080467.2:c.3276+1G= NP_001073936.1:n.3276+1G=
NM_001080467.3:c.3276+1G= MANE Select NP_001073936.1:n.3276+1G=