Canonical Allele Identifier: CA389053507
Community Standard Title: NM_000257.4(MYH7):c.209C>G (p.Thr70Ser)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433220G>C , CM000676.2:g.23433220G>C GRCh38
NC_000014.8:g.23902429G>C , CM000676.1:g.23902429G>C GRCh37
NC_000014.7:g.22972269G>C NCBI36
NG_007884.1:g.7442C>G , LRG_384:g.7442C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.209C>G MANE Select NP_000248.2:p.Thr70Ser
ENST00000355349.4:c.209C>G MANE Select ENSP00000347507.3:p.Thr70Ser
NM_000257.3:c.209C>G NP_000248.2:p.Thr70Ser
ENST00000355349.3:c.209C>G ENSP00000347507.3:p.Thr70Ser
XM_017021340.1:c.209C>G XP_016876829.1:p.Thr70Ser
XR_245686.3:n.315C>G