Canonical Allele Identifier: CA485626262
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23901051G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431842G>C , CM000676.2:g.23431842G>C GRCh38
NC_000014.8:g.23901051G>C , CM000676.1:g.23901051G>C GRCh37
NC_000014.7:g.22970891G>C NCBI36
NG_007884.1:g.8820C>G , LRG_384:g.8820C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.558C>G MANE Select ENSP00000347507.3:p.Val186=
ENST00000355349.3:c.558C>G ENSP00000347507.3:p.Val186=
NM_000257.3:c.558C>G NP_000248.2:p.Val186=
XR_245686.3:n.664C>G
XM_017021340.1:c.558C>G XP_016876829.1:p.Val186=
NM_000257.4:c.558C>G MANE Select NP_000248.2:p.Val186=