Canonical Allele Identifier: CA041383
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171380
ClinVar RCV Id: RCV001524440
dbSNP Id: rs756862819

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417611C>T , CM000676.2:g.23417611C>T GRCh38
NC_000014.8:g.23886820C>T , CM000676.1:g.23886820C>T GRCh37
NC_000014.7:g.22956660C>T NCBI36
NG_007884.1:g.23051G>A , LRG_384:g.23051G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4245G>A MANE Select ENSP00000347507.3:p.Glu1415=
ENST00000355349.3:c.4245G>A ENSP00000347507.3:p.Glu1415=
NM_000257.3:c.4245G>A NP_000248.2:p.Glu1415=
XM_017021340.1:c.4245G>A XP_016876829.1:p.Glu1415=
NM_000257.4:c.4245G>A MANE Select NP_000248.2:p.Glu1415=