Canonical Allele Identifier: CA485627003
Community Standard Title: NM_000257.4(MYH7):c.207G>C (p.Val69=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433222C>G , CM000676.2:g.23433222C>G GRCh38
NC_000014.8:g.23902431C>G , CM000676.1:g.23902431C>G GRCh37
NC_000014.7:g.22972271C>G NCBI36
NG_007884.1:g.7440G>C , LRG_384:g.7440G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.207G>C MANE Select NP_000248.2:p.Val69=
ENST00000355349.4:c.207G>C MANE Select ENSP00000347507.3:p.Val69=
NM_000257.3:c.207G>C NP_000248.2:p.Val69=
ENST00000355349.3:c.207G>C ENSP00000347507.3:p.Val69=
XM_017021340.1:c.207G>C XP_016876829.1:p.Val69=
XR_245686.3:n.313G>C