Canonical Allele Identifier: CA2123441738
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417775C= , CM000676.2:g.23417775C= GRCh38
NC_000014.8:g.23886984C= , CM000676.1:g.23886984C= GRCh37
NC_000014.7:g.22956824C= NCBI36
NG_007884.1:g.22887G= , LRG_384:g.22887G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-89G= MANE Select ENSP00000347507.3:n.4170-89G=
ENST00000355349.3:c.4170-89G= ENSP00000347507.3:n.4170-89G=
NM_000257.3:c.4170-89G= NP_000248.2:n.4170-89G=
XM_017021340.1:c.4170-89G= XP_016876829.1:n.4170-89G=
NM_000257.4:c.4170-89G= MANE Select NP_000248.2:n.4170-89G=