Canonical Allele Identifier: CA2302428761
Gene: MYO5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49878942T= , CM000680.2:g.49878942T= GRCh38
NC_000018.9:g.47405312T= , CM000680.1:g.47405312T= GRCh37
NC_000018.8:g.45659310T= NCBI36
NG_012925.1:g.321140A=
NG_012925.2:g.321140A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697218.1:n.33A=
ENST00000697219.1:c.3073+3A=
ENST00000285039.12:c.3276+3A= MANE Select ENSP00000285039.6:n.3276+3A=
ENST00000285039.11:c.3276+3A= ENSP00000285039.6:n.3276+3A=
ENST00000324581.10:c.705+3A= ENSP00000315531.7:n.705+3A=
ENST00000589568.1:n.477+3A=
ENST00000616031.4:c.1907-42209A= ENSP00000479038.1:n.1907-42209A=
NM_001080467.2:c.3276+3A= NP_001073936.1:n.3276+3A=
NM_001080467.3:c.3276+3A= MANE Select NP_001073936.1:n.3276+3A=