Canonical Allele Identifier: CA389051890
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23900148A>T (hg19) chr14:g.23430939A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23430939A>T , CM000676.2:g.23430939A>T GRCh38
NC_000014.8:g.23900148A>T , CM000676.1:g.23900148A>T GRCh37
NC_000014.7:g.22969988A>T NCBI36
NG_007884.1:g.9723T>A , LRG_384:g.9723T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.857T>A MANE Select ENSP00000347507.3:p.Phe286Tyr
ENST00000355349.3:c.857T>A ENSP00000347507.3:p.Phe286Tyr
NM_000257.3:c.857T>A NP_000248.2:p.Phe286Tyr
XR_245686.3:n.963T>A
XM_017021340.1:c.857T>A XP_016876829.1:p.Phe286Tyr
NM_000257.4:c.857T>A MANE Select NP_000248.2:p.Phe286Tyr
Search 100 bp 5'
Search 100 bp 3'