Canonical Allele Identifier: CA389043443
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773912
ClinVar RCV Id: RCV003532675
gnomAD v4: 14-23420003-C-T
MyVariant Identifiers: chr14:g.23889212C>T (hg19) chr14:g.23420003C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420003C>T , CM000676.2:g.23420003C>T GRCh38
NC_000014.8:g.23889212C>T , CM000676.1:g.23889212C>T GRCh37
NC_000014.7:g.22959052C>T NCBI36
NG_007884.1:g.20659G>A , LRG_384:g.20659G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3568G>A MANE Select ENSP00000347507.3:p.Ala1190Thr
ENST00000355349.3:c.3568G>A ENSP00000347507.3:p.Ala1190Thr
NM_000257.3:c.3568G>A NP_000248.2:p.Ala1190Thr
XM_017021340.1:c.3568G>A XP_016876829.1:p.Ala1190Thr
NM_000257.4:c.3568G>A MANE Select NP_000248.2:p.Ala1190Thr
Search 100 bp 5'
Search 100 bp 3'