Canonical Allele Identifier: CA2123414125
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23393690C= , CM000676.2:g.23393690C= GRCh38
NC_000014.8:g.23862899C= , CM000676.1:g.23862899C= GRCh37
NC_000014.7:g.22932739C= NCBI36
NG_023444.1:g.19588G= , LRG_389:g.19588G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405093.9:c.2904G= MANE Select ENSP00000386041.3:p.Lys968=
ENST00000356287.3:c.2904G= ENSP00000348634.3:p.Lys968=
ENST00000405093.7:c.2904G= ENSP00000386041.3:p.Lys968=
NM_002471.3:c.2904G= , LRG_389t1:c.2904G= NP_002462.2:p.Lys968=
NM_002471.4:c.2904G= MANE Select NP_002462.2:p.Lys968=