Canonical Allele Identifier: CA2123413469
Gene: MYH6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23392883A= , CM000676.2:g.23392883A= GRCh38
NC_000014.8:g.23862092A= , CM000676.1:g.23862092A= GRCh37
NC_000014.7:g.22931932A= NCBI36
NG_023444.1:g.20395T= , LRG_389:g.20395T=

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.3251+29T= MANE Select ENSP00000386041.3:n.3251+29T=
ENST00000356287.3:c.3251+29T= ENSP00000348634.3:n.3251+29T=
ENST00000405093.7:c.3251+29T= ENSP00000386041.3:n.3251+29T=
NM_002471.3:c.3251+29T= , LRG_389t1:c.3251+29T= NP_002462.2:n.3251+29T=
NM_002471.4:c.3251+29T= MANE Select NP_002462.2:n.3251+29T=
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