Canonical Allele Identifier: CA485626465
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23901915C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23432706C>T , CM000676.2:g.23432706C>T GRCh38
NC_000014.8:g.23901915C>T , CM000676.1:g.23901915C>T GRCh37
NC_000014.7:g.22971755C>T NCBI36
NG_007884.1:g.7956G>A , LRG_384:g.7956G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.435G>A MANE Select ENSP00000347507.3:p.Lys145=
ENST00000355349.3:c.435G>A ENSP00000347507.3:p.Lys145=
NM_000257.3:c.435G>A NP_000248.2:p.Lys145=
XR_245686.3:n.541G>A
XM_017021340.1:c.435G>A XP_016876829.1:p.Lys145=
NM_000257.4:c.435G>A MANE Select NP_000248.2:p.Lys145=
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Search 100 bp 3'