Canonical Allele Identifier: CA2624246046
Gene: MYH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23396248T>A , CM000676.2:g.23396248T>A GRCh38
NC_000014.8:g.23865457T>A , CM000676.1:g.23865457T>A GRCh37
NC_000014.7:g.22935297T>A NCBI36
NG_023444.1:g.17030A>T , LRG_389:g.17030A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405093.9:c.2429+36A>T MANE Select ENSP00000386041.3:n.2429+36A>T
ENST00000356287.3:c.2429+36A>T ENSP00000348634.3:n.2429+36A>T
ENST00000405093.7:c.2429+36A>T ENSP00000386041.3:n.2429+36A>T
NM_002471.3:c.2429+36A>T , LRG_389t1:c.2429+36A>T NP_002462.2:n.2429+36A>T
NM_002471.4:c.2429+36A>T MANE Select NP_002462.2:n.2429+36A>T