Canonical Allele Identifier: CA485611086
Community Standard Title: NM_002471.4(MYH6):c.852C>T (p.Tyr284=)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23403394G>A , CM000676.2:g.23403394G>A GRCh38
NC_000014.8:g.23872603G>A , CM000676.1:g.23872603G>A GRCh37
NC_000014.7:g.22942443G>A NCBI36
NG_023444.1:g.9884C>T , LRG_389:g.9884C>T

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.852C>T MANE Select NP_002462.2:p.Tyr284=
ENST00000405093.9:c.852C>T MANE Select ENSP00000386041.3:p.Tyr284=
NM_002471.3:c.852C>T , LRG_389t1:c.852C>T NP_002462.2:p.Tyr284=
ENST00000356287.3:c.852C>T ENSP00000348634.3:p.Tyr284=
ENST00000405093.7:c.852C>T ENSP00000386041.3:p.Tyr284=
ENST00000557461.1:n.906C>T
ENST00000557461.2:n.919C>T