Canonical Allele Identifier: CA485767259
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23900661T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431452T>A , CM000676.2:g.23431452T>A GRCh38
NC_000014.8:g.23900661T>A , CM000676.1:g.23900661T>A GRCh37
NC_000014.7:g.22970501T>A NCBI36
NG_007884.1:g.9210A>T , LRG_384:g.9210A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.762A>T MANE Select ENSP00000347507.3:p.Ala254=
ENST00000355349.3:c.762A>T ENSP00000347507.3:p.Ala254=
NM_000257.3:c.762A>T NP_000248.2:p.Ala254=
XR_245686.3:n.868A>T
XM_017021340.1:c.762A>T XP_016876829.1:p.Ala254=
NM_000257.4:c.762A>T MANE Select NP_000248.2:p.Ala254=
Search 100 bp 5'
Search 100 bp 3'