Canonical Allele Identifier: CA389042800
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2448066
ClinVar RCV Id: RCV003168160
MyVariant Identifiers: chr14:g.23888805T>A (hg19) chr14:g.23419596T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419596T>A , CM000676.2:g.23419596T>A GRCh38
NC_000014.8:g.23888805T>A , CM000676.1:g.23888805T>A GRCh37
NC_000014.7:g.22958645T>A NCBI36
NG_007884.1:g.21066A>T , LRG_384:g.21066A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3740A>T MANE Select ENSP00000347507.3:p.Lys1247Met
ENST00000355349.3:c.3740A>T ENSP00000347507.3:p.Lys1247Met
NM_000257.3:c.3740A>T NP_000248.2:p.Lys1247Met
XM_017021340.1:c.3740A>T XP_016876829.1:p.Lys1247Met
NM_000257.4:c.3740A>T MANE Select NP_000248.2:p.Lys1247Met
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