Canonical Allele Identifier: CA485767366
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23900878C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431669C>A , CM000676.2:g.23431669C>A GRCh38
NC_000014.8:g.23900878C>A , CM000676.1:g.23900878C>A GRCh37
NC_000014.7:g.22970718C>A NCBI36
NG_007884.1:g.8993G>T , LRG_384:g.8993G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.648G>T MANE Select ENSP00000347507.3:p.Leu216=
ENST00000355349.3:c.648G>T ENSP00000347507.3:p.Leu216=
NM_000257.3:c.648G>T NP_000248.2:p.Leu216=
XR_245686.3:n.754G>T
XM_017021340.1:c.648G>T XP_016876829.1:p.Leu216=
NM_000257.4:c.648G>T MANE Select NP_000248.2:p.Leu216=
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Search 100 bp 3'