Canonical Allele Identifier: CA2302428762
Gene: MYO5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49878943G= , CM000680.2:g.49878943G= GRCh38
NC_000018.9:g.47405313G= , CM000680.1:g.47405313G= GRCh37
NC_000018.8:g.45659311G= NCBI36
NG_012925.1:g.321139C=
NG_012925.2:g.321139C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697218.1:n.32C=
ENST00000697219.1:c.3073+2C=
ENST00000285039.12:c.3276+2C= MANE Select ENSP00000285039.6:n.3276+2C=
ENST00000285039.11:c.3276+2C= ENSP00000285039.6:n.3276+2C=
ENST00000324581.10:c.705+2C= ENSP00000315531.7:n.705+2C=
ENST00000589568.1:n.477+2C=
ENST00000616031.4:c.1907-42210C= ENSP00000479038.1:n.1907-42210C=
NM_001080467.2:c.3276+2C= NP_001073936.1:n.3276+2C=
NM_001080467.3:c.3276+2C= MANE Select NP_001073936.1:n.3276+2C=