Canonical Allele Identifier: CA389053156
Community Standard Title: NM_000257.4(MYH7):c.302T>G (p.Val101Gly)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433127A>C , CM000676.2:g.23433127A>C GRCh38
NC_000014.8:g.23902336A>C , CM000676.1:g.23902336A>C GRCh37
NC_000014.7:g.22972176A>C NCBI36
NG_007884.1:g.7535T>G , LRG_384:g.7535T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.302T>G MANE Select NP_000248.2:p.Val101Gly
ENST00000355349.4:c.302T>G MANE Select ENSP00000347507.3:p.Val101Gly
NM_000257.3:c.302T>G NP_000248.2:p.Val101Gly
ENST00000355349.3:c.302T>G ENSP00000347507.3:p.Val101Gly
XM_017021340.1:c.302T>G XP_016876829.1:p.Val101Gly
XR_245686.3:n.408T>G