Canonical Allele Identifier: CA2573149835
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1615682
ClinVar RCV Id: RCV002074718
dbSNP Id: rs2138652094
gnomAD v4: 14-23419471-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419471C>T , CM000676.2:g.23419471C>T GRCh38
NC_000014.8:g.23888680C>T , CM000676.1:g.23888680C>T GRCh37
NC_000014.7:g.22958520C>T NCBI36
NG_007884.1:g.21191G>A , LRG_384:g.21191G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3853+12G>A MANE Select ENSP00000347507.3:n.3853+12G>A
ENST00000355349.3:c.3853+12G>A ENSP00000347507.3:n.3853+12G>A
NM_000257.3:c.3853+12G>A NP_000248.2:n.3853+12G>A
XM_017021340.1:c.3853+12G>A XP_016876829.1:n.3853+12G>A
NM_000257.4:c.3853+12G>A MANE Select NP_000248.2:n.3853+12G>A
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