Canonical Allele Identifier: CA134313
Community Standard Title: NM_002471.4(MYH6):c.3199A>G (p.Ser1067Gly)
Gene: MYH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23392964T>C , CM000676.2:g.23392964T>C GRCh38
NC_000014.8:g.23862173T>C , CM000676.1:g.23862173T>C GRCh37
NC_000014.7:g.22932013T>C NCBI36
NG_023444.1:g.20314A>G , LRG_389:g.20314A>G

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.3199A>G MANE Select NP_002462.2:p.Ser1067Gly
ENST00000405093.9:c.3199A>G MANE Select ENSP00000386041.3:p.Ser1067Gly
NM_002471.3:c.3199A>G , LRG_389t1:c.3199A>G NP_002462.2:p.Ser1067Gly
ENST00000356287.3:c.3199A>G ENSP00000348634.3:p.Ser1067Gly
ENST00000405093.7:c.3199A>G ENSP00000386041.3:p.Ser1067Gly