Canonical Allele Identifier: CA2123418149
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23396444C= , CM000676.2:g.23396444C= GRCh38
NC_000014.8:g.23865653C= , CM000676.1:g.23865653C= GRCh37
NC_000014.7:g.22935493C= NCBI36
NG_023444.1:g.16834G= , LRG_389:g.16834G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405093.9:c.2293-24G= MANE Select ENSP00000386041.3:n.2293-24G=
ENST00000356287.3:c.2293-24G= ENSP00000348634.3:n.2293-24G=
ENST00000405093.7:c.2293-24G= ENSP00000386041.3:n.2293-24G=
NM_002471.3:c.2293-24G= , LRG_389t1:c.2293-24G= NP_002462.2:n.2293-24G=
NM_002471.4:c.2293-24G= MANE Select NP_002462.2:n.2293-24G=