Canonical Allele Identifier: CA389053141
Community Standard Title: NM_000257.4(MYH7):c.308A>G (p.Tyr103Cys)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433121T>C , CM000676.2:g.23433121T>C GRCh38
NC_000014.8:g.23902330T>C , CM000676.1:g.23902330T>C GRCh37
NC_000014.7:g.22972170T>C NCBI36
NG_007884.1:g.7541A>G , LRG_384:g.7541A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.308A>G MANE Select NP_000248.2:p.Tyr103Cys
ENST00000355349.4:c.308A>G MANE Select ENSP00000347507.3:p.Tyr103Cys
NM_000257.3:c.308A>G NP_000248.2:p.Tyr103Cys
ENST00000355349.3:c.308A>G ENSP00000347507.3:p.Tyr103Cys
XM_017021340.1:c.308A>G XP_016876829.1:p.Tyr103Cys
XR_245686.3:n.414A>G