Canonical Allele Identifier: CA389050781
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23898207T>A (hg19) chr14:g.23428998T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23428998T>A , CM000676.2:g.23428998T>A GRCh38
NC_000014.8:g.23898207T>A , CM000676.1:g.23898207T>A GRCh37
NC_000014.7:g.22968047T>A NCBI36
NG_007884.1:g.11664A>T , LRG_384:g.11664A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1364A>T MANE Select ENSP00000347507.3:p.Tyr455Phe
ENST00000355349.3:c.1364A>T ENSP00000347507.3:p.Tyr455Phe
NM_000257.3:c.1364A>T NP_000248.2:p.Tyr455Phe
XR_245686.3:n.1470A>T
XM_017021340.1:c.1364A>T XP_016876829.1:p.Tyr455Phe
NM_000257.4:c.1364A>T MANE Select NP_000248.2:p.Tyr455Phe
Search 100 bp 5'
Search 100 bp 3'