Canonical Allele Identifier: CA389053146
Community Standard Title: NM_000257.4(MYH7):c.307T>A (p.Tyr103Asn)
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433122A>T , CM000676.2:g.23433122A>T GRCh38
NC_000014.8:g.23902331A>T , CM000676.1:g.23902331A>T GRCh37
NC_000014.7:g.22972171A>T NCBI36
NG_007884.1:g.7540T>A , LRG_384:g.7540T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000257.4:c.307T>A MANE Select NP_000248.2:p.Tyr103Asn
ENST00000355349.4:c.307T>A MANE Select ENSP00000347507.3:p.Tyr103Asn
NM_000257.3:c.307T>A NP_000248.2:p.Tyr103Asn
ENST00000355349.3:c.307T>A ENSP00000347507.3:p.Tyr103Asn
XM_017021340.1:c.307T>A XP_016876829.1:p.Tyr103Asn
XR_245686.3:n.413T>A