Canonical Allele Identifier: CA485766806
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23895180G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23425971G>T , CM000676.2:g.23425971G>T GRCh38
NC_000014.8:g.23895180G>T , CM000676.1:g.23895180G>T GRCh37
NC_000014.7:g.22965020G>T NCBI36
NG_007884.1:g.14691C>A , LRG_384:g.14691C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2155C>A MANE Select ENSP00000347507.3:p.Arg719=
ENST00000355349.3:c.2155C>A ENSP00000347507.3:p.Arg719=
NM_000257.3:c.2155C>A NP_000248.2:p.Arg719=
XR_245686.3:n.2261C>A
XM_017021340.1:c.2155C>A XP_016876829.1:p.Arg719=
NM_000257.4:c.2155C>A MANE Select NP_000248.2:p.Arg719=