Canonical Allele Identifier: CA1392092226
Gene: MYH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.108524704G= , CM000665.2:g.108524704G= GRCh38
NC_000003.11:g.108243551G= , CM000665.1:g.108243551G= GRCh37
NC_000003.10:g.109726241G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273353.5:c.-58+4559C= ENSP00000273353.4:n.-58+4559C=
ENST00000273353.4:c.3+4559C= ENSP00000273353.3:n.3+4559C=
ENST00000273353.3:c.3+4559C= ENSP00000273353.3:n.3+4559C=
NM_014981.1:c.3+4559C= NP_055796.1:n.3+4559C=
XM_011512559.1:c.3+4559C= XP_011510861.1:n.3+4559C=
XM_011512559.2:c.3+4559C= XP_011510861.1:n.3+4559C=
NM_014981.2:c.3+4559C= NP_055796.1:n.3+4559C=