Canonical Allele Identifier: CA485766473
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 921050
ClinVar RCV Id: RCV001180194 RCV001460278
dbSNP Id: rs1892207214
MyVariant Identifiers: chr14:g.23885501C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416292C>T , CM000676.2:g.23416292C>T GRCh38
NC_000014.8:g.23885501C>T , CM000676.1:g.23885501C>T GRCh37
NC_000014.7:g.22955341C>T NCBI36
NG_007884.1:g.24370G>A , LRG_384:g.24370G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4665G>A (MYH7) MANE Select ENSP00000347507.3:p.Glu1555=
ENST00000355349.3:c.4665G>A (MYH7) ENSP00000347507.3:p.Glu1555=
NM_000257.3:c.4665G>A (MYH7) NP_000248.2:p.Glu1555=
NR_126491.1:n.553C>T (MHRT)
XM_017021340.1:c.4665G>A (MYH7) XP_016876829.1:p.Glu1555=
NM_000257.4:c.4665G>A (MYH7) MANE Select NP_000248.2:p.Glu1555=
Search 100 bp 5'
Search 100 bp 3'