Canonical Allele Identifier: CA2123461888
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415084T= , CM000676.2:g.23415084T= GRCh38
NC_000014.8:g.23884293T= , CM000676.1:g.23884293T= GRCh37
NC_000014.7:g.22954133T= NCBI36
NG_007884.1:g.25578A= , LRG_384:g.25578A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5470A= MANE Select ENSP00000347507.3:p.Asn1824=
ENST00000355349.3:c.5470A= ENSP00000347507.3:p.Asn1824=
NM_000257.3:c.5470A= NP_000248.2:p.Asn1824=
XM_017021340.1:c.5470A= XP_016876829.1:p.Asn1824=
NM_000257.4:c.5470A= MANE Select NP_000248.2:p.Asn1824=