Canonical Allele Identifier: CA2123418230

Gene: MYH6

Linked Data

• dbSNP Id: rs1891400489
• gnomAD v4: 14-23396506-C-CCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23396509_23396511dup , CM000676.2:g.23396509_23396511dup	GRCh38
NC_000014.8:g.23865718_23865720dup , CM000676.1:g.23865718_23865720dup	GRCh37
NC_000014.7:g.22935558_22935560dup	NCBI36
NG_023444.1:g.16769_16771dup , LRG_389:g.16769_16771dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405093.9:c.2293-89_2293-87dup MANE Select	ENSP00000386041.3:n.2293-89_2293-87dup
ENST00000356287.3:c.2293-89_2293-87dup	ENSP00000348634.3:n.2293-89_2293-87dup
ENST00000405093.7:c.2293-89_2293-87dup	ENSP00000386041.3:n.2293-89_2293-87dup
NM_002471.3:c.2293-89_2293-87dup , LRG_389t1:c.2293-89_2293-87dup	NP_002462.2:n.2293-89_2293-87dup
NM_002471.4:c.2293-89_2293-87dup MANE Select	NP_002462.2:n.2293-89_2293-87dup