Canonical Allele Identifier: CA10581177
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 235026
ClinVar RCV Id: RCV000223878 RCV000818531 RCV002378957
dbSNP Id: rs397516101
MyVariant Identifiers: chr14:g.23898213C>A (hg19) chr14:g.23429004C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429004C>A , CM000676.2:g.23429004C>A GRCh38
NC_000014.8:g.23898213C>A , CM000676.1:g.23898213C>A GRCh37
NC_000014.7:g.22968053C>A NCBI36
NG_007884.1:g.11658G>T , LRG_384:g.11658G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1358G>T MANE Select ENSP00000347507.3:p.Arg453Leu
ENST00000355349.3:c.1358G>T ENSP00000347507.3:p.Arg453Leu
NM_000257.3:c.1358G>T NP_000248.2:p.Arg453Leu
XR_245686.3:n.1464G>T
XM_017021340.1:c.1358G>T XP_016876829.1:p.Arg453Leu
NM_000257.4:c.1358G>T MANE Select NP_000248.2:p.Arg453Leu
Search 100 bp 5'
Search 100 bp 3'