Canonical Allele Identifier: CA2123450900
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431152G= , CM000676.2:g.23431152G= GRCh38
NC_000014.8:g.23900361G= , CM000676.1:g.23900361G= GRCh37
NC_000014.7:g.22970201G= NCBI36
NG_007884.1:g.9510C= , LRG_384:g.9510C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-153C= MANE Select ENSP00000347507.3:n.797-153C=
ENST00000355349.3:c.797-153C= ENSP00000347507.3:n.797-153C=
NM_000257.3:c.797-153C= NP_000248.2:n.797-153C=
XR_245686.3:n.903-153C=
XM_017021340.1:c.797-153C= XP_016876829.1:n.797-153C=
NM_000257.4:c.797-153C= MANE Select NP_000248.2:n.797-153C=