Canonical Allele Identifier: CA485616148
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23883070G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413861G>A , CM000676.2:g.23413861G>A GRCh38
NC_000014.8:g.23883070G>A , CM000676.1:g.23883070G>A GRCh37
NC_000014.7:g.22952910G>A NCBI36
NG_007884.1:g.26801C>T , LRG_384:g.26801C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5688C>T MANE Select ENSP00000347507.3:p.Phe1896=
ENST00000355349.3:c.5688C>T ENSP00000347507.3:p.Phe1896=
NM_000257.3:c.5688C>T NP_000248.2:p.Phe1896=
XM_017021340.1:c.5688C>T XP_016876829.1:p.Phe1896=
NM_000257.4:c.5688C>T MANE Select NP_000248.2:p.Phe1896=
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