Canonical Allele Identifier: CA2123414031
Gene: MYH6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23393625T= , CM000676.2:g.23393625T= GRCh38
NC_000014.8:g.23862834T= , CM000676.1:g.23862834T= GRCh37
NC_000014.7:g.22932674T= NCBI36
NG_023444.1:g.19653A= , LRG_389:g.19653A=

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.2928+41A= MANE Select ENSP00000386041.3:n.2928+41A=
ENST00000356287.3:c.2928+41A= ENSP00000348634.3:n.2928+41A=
ENST00000405093.7:c.2928+41A= ENSP00000386041.3:n.2928+41A=
NM_002471.3:c.2928+41A= , LRG_389t1:c.2928+41A= NP_002462.2:n.2928+41A=
NM_002471.4:c.2928+41A= MANE Select NP_002462.2:n.2928+41A=
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