Canonical Allele Identifier: CA2123455162
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424420T= , CM000676.2:g.23424420T= GRCh38
NC_000014.8:g.23893629T= , CM000676.1:g.23893629T= GRCh37
NC_000014.7:g.22963469T= NCBI36
NG_007884.1:g.16242A= , LRG_384:g.16242A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-271A= MANE Select ENSP00000347507.3:n.2680-271A=
ENST00000355349.3:c.2680-271A= ENSP00000347507.3:n.2680-271A=
NM_000257.3:c.2680-271A= NP_000248.2:n.2680-271A=
XR_245686.3:n.2786-271A=
XM_017021340.1:c.2680-271A= XP_016876829.1:n.2680-271A=
NM_000257.4:c.2680-271A= MANE Select NP_000248.2:n.2680-271A=