Canonical Allele Identifier: CA7115519
Gene: MYH6 HGNC NCBI

Linked Data

dbSNP Id: rs775654359
ExAC: 14:23865857 A / T
gnomAD v2: 14-23865857-A-T
gnomAD v3: 14-23396648-A-T
gnomAD v4: 14-23396648-A-T
MyVariant Identifiers: chr14:g.23865857A>T (hg19) chr14:g.23396648A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23396648A>T , CM000676.2:g.23396648A>T GRCh38
NC_000014.8:g.23865857A>T , CM000676.1:g.23865857A>T GRCh37
NC_000014.7:g.22935697A>T NCBI36
NG_023444.1:g.16630T>A , LRG_389:g.16630T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405093.9:c.2292+46T>A MANE Select ENSP00000386041.3:n.2292+46T>A
ENST00000356287.3:c.2292+46T>A ENSP00000348634.3:n.2292+46T>A
ENST00000405093.7:c.2292+46T>A ENSP00000386041.3:n.2292+46T>A
NM_002471.3:c.2292+46T>A , LRG_389t1:c.2292+46T>A NP_002462.2:n.2292+46T>A
NM_002471.4:c.2292+46T>A MANE Select NP_002462.2:n.2292+46T>A
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