Canonical Allele Identifier: CA2123418265
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23396544T= , CM000676.2:g.23396544T= GRCh38
NC_000014.8:g.23865753T= , CM000676.1:g.23865753T= GRCh37
NC_000014.7:g.22935593T= NCBI36
NG_023444.1:g.16734A= , LRG_389:g.16734A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405093.9:c.2293-124A= MANE Select ENSP00000386041.3:n.2293-124A=
ENST00000356287.3:c.2293-124A= ENSP00000348634.3:n.2293-124A=
ENST00000405093.7:c.2293-124A= ENSP00000386041.3:n.2293-124A=
NM_002471.3:c.2293-124A= , LRG_389t1:c.2293-124A= NP_002462.2:n.2293-124A=
NM_002471.4:c.2293-124A= MANE Select NP_002462.2:n.2293-124A=