Canonical Allele Identifier: CA485766478

Linked Data

dbSNP Id: rs143471552

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416301C>T , CM000676.2:g.23416301C>T GRCh38
NC_000014.8:g.23885510C>T , CM000676.1:g.23885510C>T GRCh37
NC_000014.7:g.22955350C>T NCBI36
NG_007884.1:g.24361G>A , LRG_384:g.24361G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4656G>A (MYH7) MANE Select ENSP00000347507.3:p.Glu1552=
ENST00000355349.3:c.4656G>A (MYH7) ENSP00000347507.3:p.Glu1552=
NM_000257.3:c.4656G>A (MYH7) NP_000248.2:p.Glu1552=
NR_126491.1:n.558+4C>T (MHRT)
XM_017021340.1:c.4656G>A (MYH7) XP_016876829.1:p.Glu1552=
NM_000257.4:c.4656G>A (MYH7) MANE Select NP_000248.2:p.Glu1552=