Canonical Allele Identifier: CA389019025
Community Standard Title: NM_002471.4(MYH6):c.2064C>G (p.Asn688Lys)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23397067G>C , CM000676.2:g.23397067G>C GRCh38
NC_000014.8:g.23866276G>C , CM000676.1:g.23866276G>C GRCh37
NC_000014.7:g.22936116G>C NCBI36
NG_023444.1:g.16211C>G , LRG_389:g.16211C>G

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.2064C>G MANE Select NP_002462.2:p.Asn688Lys
ENST00000405093.9:c.2064C>G MANE Select ENSP00000386041.3:p.Asn688Lys
NM_002471.3:c.2064C>G , LRG_389t1:c.2064C>G NP_002462.2:p.Asn688Lys
ENST00000356287.3:c.2064C>G ENSP00000348634.3:p.Asn688Lys
ENST00000405093.7:c.2064C>G ENSP00000386041.3:p.Asn688Lys