Canonical Allele Identifier: CA485621331
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1731311
ClinVar RCV Id: RCV002333006
dbSNP Id: rs1298480275
gnomAD v2: 14-23889354-C-T
gnomAD v4: 14-23420145-C-T
MyVariant Identifiers: chr14:g.23889354C>T (hg19) chr14:g.23420145C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420145C>T , CM000676.2:g.23420145C>T GRCh38
NC_000014.8:g.23889354C>T , CM000676.1:g.23889354C>T GRCh37
NC_000014.7:g.22959194C>T NCBI36
NG_007884.1:g.20517G>A , LRG_384:g.20517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3426G>A MANE Select ENSP00000347507.3:p.Glu1142=
ENST00000355349.3:c.3426G>A ENSP00000347507.3:p.Glu1142=
NM_000257.3:c.3426G>A NP_000248.2:p.Glu1142=
XM_017021340.1:c.3426G>A XP_016876829.1:p.Glu1142=
NM_000257.4:c.3426G>A MANE Select NP_000248.2:p.Glu1142=
Search 100 bp 5'
Search 100 bp 3'