Canonical Allele Identifier: CA7115264
Gene: MYH6 HGNC NCBI

Linked Data

dbSNP Id: rs770085114
ExAC: 14:23862077 C / A
gnomAD v2: 14-23862077-C-A
gnomAD v3: 14-23392868-C-A
gnomAD v4: 14-23392868-C-A
MyVariant Identifiers: chr14:g.23862077C>A (hg19) chr14:g.23392868C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23392868C>A , CM000676.2:g.23392868C>A GRCh38
NC_000014.8:g.23862077C>A , CM000676.1:g.23862077C>A GRCh37
NC_000014.7:g.22931917C>A NCBI36
NG_023444.1:g.20410G>T , LRG_389:g.20410G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405093.9:c.3251+44G>T MANE Select ENSP00000386041.3:n.3251+44G>T
ENST00000356287.3:c.3251+44G>T ENSP00000348634.3:n.3251+44G>T
ENST00000405093.7:c.3251+44G>T ENSP00000386041.3:n.3251+44G>T
NM_002471.3:c.3251+44G>T , LRG_389t1:c.3251+44G>T NP_002462.2:n.3251+44G>T
NM_002471.4:c.3251+44G>T MANE Select NP_002462.2:n.3251+44G>T
Search 100 bp 5'
Search 100 bp 3'