Canonical Allele Identifier: CA2624255177
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23433848-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433848T>A , CM000676.2:g.23433848T>A GRCh38
NC_000014.8:g.23903057T>A , CM000676.1:g.23903057T>A GRCh37
NC_000014.7:g.22972897T>A NCBI36
NG_007884.1:g.6814A>T , LRG_384:g.6814A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-8-108A>T MANE Select ENSP00000347507.3:n.-8-108A>T
ENST00000355349.3:c.-8-108A>T ENSP00000347507.3:n.-8-108A>T
NM_000257.3:c.-8-108A>T NP_000248.2:n.-8-108A>T
XR_245686.3:n.99-108A>T
XM_017021340.1:c.-8-108A>T XP_016876829.1:n.-8-108A>T
NM_000257.4:c.-8-108A>T MANE Select NP_000248.2:n.-8-108A>T
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