Canonical Allele Identifier: CA2123462719
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415269G= , CM000676.2:g.23415269G= GRCh38
NC_000014.8:g.23884478G= , CM000676.1:g.23884478G= GRCh37
NC_000014.7:g.22954318G= NCBI36
NG_007884.1:g.25393C= , LRG_384:g.25393C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5285C= MANE Select ENSP00000347507.3:p.Ala1762=
ENST00000355349.3:c.5285C= ENSP00000347507.3:p.Ala1762=
NM_000257.3:c.5285C= NP_000248.2:p.Ala1762=
XM_017021340.1:c.5285C= XP_016876829.1:p.Ala1762=
NM_000257.4:c.5285C= MANE Select NP_000248.2:p.Ala1762=