Canonical Allele Identifier: CA10581170
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 235033
ClinVar RCV Id: RCV000223760 RCV000241907 RCV000689327 RCV001798726
dbSNP Id: rs876657884
MyVariant Identifiers: chr14:g.23886479C>T (hg19) chr14:g.23417270C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417270C>T , CM000676.2:g.23417270C>T GRCh38
NC_000014.8:g.23886479C>T , CM000676.1:g.23886479C>T GRCh37
NC_000014.7:g.22956319C>T NCBI36
NG_007884.1:g.23392G>A , LRG_384:g.23392G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.4402G>A (MYH7) MANE Select ENSP00000347507.3:p.Glu1468Lys
ENST00000355349.3:c.4402G>A (MYH7) ENSP00000347507.3:p.Glu1468Lys
NM_000257.3:c.4402G>A (MYH7) NP_000248.2:p.Glu1468Lys
NR_126491.1:n.710C>T (MHRT)
XM_017021340.1:c.4402G>A (MYH7) XP_016876829.1:p.Glu1468Lys
NM_000257.4:c.4402G>A (MYH7) MANE Select NP_000248.2:p.Glu1468Lys
Search 100 bp 5'
Search 100 bp 3'