Canonical Allele Identifier: CA485767355
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892946587
MyVariant Identifiers: chr14:g.23900854G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431645G>A , CM000676.2:g.23431645G>A GRCh38
NC_000014.8:g.23900854G>A , CM000676.1:g.23900854G>A GRCh37
NC_000014.7:g.22970694G>A NCBI36
NG_007884.1:g.9017C>T , LRG_384:g.9017C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.672C>T MANE Select ENSP00000347507.3:p.Asn224=
ENST00000355349.3:c.672C>T ENSP00000347507.3:p.Asn224=
NM_000257.3:c.672C>T NP_000248.2:p.Asn224=
XR_245686.3:n.778C>T
XM_017021340.1:c.672C>T XP_016876829.1:p.Asn224=
NM_000257.4:c.672C>T MANE Select NP_000248.2:p.Asn224=
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