Canonical Allele Identifier: CA961074473
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892562169
gnomAD v3: 14-23423441-AC-A
gnomAD v4: 14-23423441-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423442del , CM000676.2:g.23423442del GRCh38
NC_000014.8:g.23892651del , CM000676.1:g.23892651del GRCh37
NC_000014.7:g.22962491del NCBI36
NG_007884.1:g.17220del , LRG_384:g.17220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+105del MANE Select ENSP00000347507.3:n.3099+105del
ENST00000355349.3:c.3099+105del ENSP00000347507.3:n.3099+105del
NM_000257.3:c.3099+105del NP_000248.2:n.3099+105del
XR_245686.3:n.3205+105del
XM_017021340.1:c.3099+105del XP_016876829.1:n.3099+105del
NM_000257.4:c.3099+105del MANE Select NP_000248.2:n.3099+105del
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