Canonical Allele Identifier: CA2123458645
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413882G= , CM000676.2:g.23413882G= GRCh38
NC_000014.8:g.23883091G= , CM000676.1:g.23883091G= GRCh37
NC_000014.7:g.22952931G= NCBI36
NG_007884.1:g.26780C= , LRG_384:g.26780C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5667C= MANE Select ENSP00000347507.3:p.Ala1889=
ENST00000355349.3:c.5667C= ENSP00000347507.3:p.Ala1889=
NM_000257.3:c.5667C= NP_000248.2:p.Ala1889=
XM_017021340.1:c.5667C= XP_016876829.1:p.Ala1889=
NM_000257.4:c.5667C= MANE Select NP_000248.2:p.Ala1889=