Canonical Allele Identifier: CA134466
Community Standard Title: NM_002471.4(MYH6):c.5293G>A (p.Ala1765Thr)
Gene: MYH6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23384714C>T , CM000676.2:g.23384714C>T GRCh38
NC_000014.8:g.23853923C>T , CM000676.1:g.23853923C>T GRCh37
NC_000014.7:g.22923763C>T NCBI36
NG_023444.1:g.28564G>A , LRG_389:g.28564G>A

Transcript Alleles

HGVS Amino-acid Change
NM_002471.4:c.5293G>A MANE Select NP_002462.2:p.Ala1765Thr
ENST00000405093.9:c.5293G>A MANE Select ENSP00000386041.3:p.Ala1765Thr
NM_002471.3:c.5293G>A , LRG_389t1:c.5293G>A NP_002462.2:p.Ala1765Thr
ENST00000356287.3:c.5293G>A ENSP00000348634.3:p.Ala1765Thr
ENST00000405093.7:c.5293G>A ENSP00000386041.3:p.Ala1765Thr
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