Canonical Allele Identifier: CA014078
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42974
dbSNP Id: rs149103761

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419559G>A , CM000676.2:g.23419559G>A GRCh38
NC_000014.8:g.23888768G>A , CM000676.1:g.23888768G>A GRCh37
NC_000014.7:g.22958608G>A NCBI36
NG_007884.1:g.21103C>T , LRG_384:g.21103C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3777C>T MANE Select ENSP00000347507.3:p.His1259=
ENST00000355349.3:c.3777C>T ENSP00000347507.3:p.His1259=
NM_000257.3:c.3777C>T NP_000248.2:p.His1259=
XM_017021340.1:c.3777C>T XP_016876829.1:p.His1259=
NM_000257.4:c.3777C>T MANE Select NP_000248.2:p.His1259=