Canonical Allele Identifier: CA389045738
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 810738
ClinVar RCV Id: RCV000999572
dbSNP Id: rs1595081245
MyVariant Identifiers: chr14:g.23892791T>C (hg19) chr14:g.23423582T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423582T>C , CM000676.2:g.23423582T>C GRCh38
NC_000014.8:g.23892791T>C , CM000676.1:g.23892791T>C GRCh37
NC_000014.7:g.22962631T>C NCBI36
NG_007884.1:g.17080A>G , LRG_384:g.17080A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3064A>G MANE Select ENSP00000347507.3:p.Lys1022Glu
ENST00000355349.3:c.3064A>G ENSP00000347507.3:p.Lys1022Glu
NM_000257.3:c.3064A>G NP_000248.2:p.Lys1022Glu
XR_245686.3:n.3170A>G
XM_017021340.1:c.3064A>G XP_016876829.1:p.Lys1022Glu
NM_000257.4:c.3064A>G MANE Select NP_000248.2:p.Lys1022Glu
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