Canonical Allele Identifier: CA389052038
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431418A>T , CM000676.2:g.23431418A>T GRCh38
NC_000014.8:g.23900627A>T , CM000676.1:g.23900627A>T GRCh37
NC_000014.7:g.22970467A>T NCBI36
NG_007884.1:g.9244T>A , LRG_384:g.9244T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.796T>A MANE Select ENSP00000347507.3:p.Tyr266Asn
ENST00000355349.3:c.796T>A ENSP00000347507.3:p.Tyr266Asn
NM_000257.3:c.796T>A NP_000248.2:p.Tyr266Asn
XR_245686.3:n.902T>A
XM_017021340.1:c.796T>A XP_016876829.1:p.Tyr266Asn
NM_000257.4:c.796T>A MANE Select NP_000248.2:p.Tyr266Asn