Canonical Allele Identifier: CA485627109
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23902768T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433559T>C , CM000676.2:g.23433559T>C GRCh38
NC_000014.8:g.23902768T>C , CM000676.1:g.23902768T>C GRCh37
NC_000014.7:g.22972608T>C NCBI36
NG_007884.1:g.7103A>G , LRG_384:g.7103A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.174A>G MANE Select ENSP00000347507.3:p.Lys58=
ENST00000355349.3:c.174A>G ENSP00000347507.3:p.Lys58=
NM_000257.3:c.174A>G NP_000248.2:p.Lys58=
XR_245686.3:n.280A>G
XM_017021340.1:c.174A>G XP_016876829.1:p.Lys58=
NM_000257.4:c.174A>G MANE Select NP_000248.2:p.Lys58=