Canonical Allele Identifier: CA485621405
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773929
ClinVar RCV Id: RCV003532692
MyVariant Identifiers: chr14:g.23889417C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420208C>T , CM000676.2:g.23420208C>T GRCh38
NC_000014.8:g.23889417C>T , CM000676.1:g.23889417C>T GRCh37
NC_000014.7:g.22959257C>T NCBI36
NG_007884.1:g.20454G>A , LRG_384:g.20454G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3363G>A MANE Select ENSP00000347507.3:p.Glu1121=
ENST00000355349.3:c.3363G>A ENSP00000347507.3:p.Glu1121=
NM_000257.3:c.3363G>A NP_000248.2:p.Glu1121=
XR_245686.3:n.3471G>A
XM_017021340.1:c.3363G>A XP_016876829.1:p.Glu1121=
NM_000257.4:c.3363G>A MANE Select NP_000248.2:p.Glu1121=
Search 100 bp 5'
Search 100 bp 3'