Canonical Allele Identifier: CA485616052
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23882974G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23413765G>C , CM000676.2:g.23413765G>C GRCh38
NC_000014.8:g.23882974G>C , CM000676.1:g.23882974G>C GRCh37
NC_000014.7:g.22952814G>C NCBI36
NG_007884.1:g.26897C>G , LRG_384:g.26897C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5784C>G MANE Select ENSP00000347507.3:p.Gly1928=
ENST00000355349.3:c.5784C>G ENSP00000347507.3:p.Gly1928=
NM_000257.3:c.5784C>G NP_000248.2:p.Gly1928=
XM_017021340.1:c.5784C>G XP_016876829.1:p.Gly1928=
NM_000257.4:c.5784C>G MANE Select NP_000248.2:p.Gly1928=
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