Canonical Allele Identifier: CA2123454861
Community Standard Title: NM_000257.4(MYH7):c.298G= (p.Ala100=)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433131C= , CM000676.2:g.23433131C= GRCh38
NC_000014.8:g.23902340C= , CM000676.1:g.23902340C= GRCh37
NC_000014.7:g.22972180C= NCBI36
NG_007884.1:g.7531G= , LRG_384:g.7531G=

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.298G= MANE Select NP_000248.2:p.Ala100=
ENST00000355349.4:c.298G= MANE Select ENSP00000347507.3:p.Ala100=
NM_000257.3:c.298G= NP_000248.2:p.Ala100=
ENST00000355349.3:c.298G= ENSP00000347507.3:p.Ala100=
XM_017021340.1:c.298G= XP_016876829.1:p.Ala100=
XR_245686.3:n.404G=