Canonical Allele Identifier: CA2123441234
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417631C= , CM000676.2:g.23417631C= GRCh38
NC_000014.8:g.23886840C= , CM000676.1:g.23886840C= GRCh37
NC_000014.7:g.22956680C= NCBI36
NG_007884.1:g.23031G= , LRG_384:g.23031G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4225G= MANE Select ENSP00000347507.3:p.Ala1409=
ENST00000355349.3:c.4225G= ENSP00000347507.3:p.Ala1409=
NM_000257.3:c.4225G= NP_000248.2:p.Ala1409=
XM_017021340.1:c.4225G= XP_016876829.1:p.Ala1409=
NM_000257.4:c.4225G= MANE Select NP_000248.2:p.Ala1409=