Canonical Allele Identifier: CA16606527
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 383852
ClinVar RCV Id: RCV000418757 RCV001187669 RCV003748228
dbSNP Id: rs1057521761
gnomAD v4: 14-23416157-G-A
MyVariant Identifiers: chr14:g.23885366G>A (hg19) chr14:g.23416157G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416157G>A , CM000676.2:g.23416157G>A GRCh38
NC_000014.8:g.23885366G>A , CM000676.1:g.23885366G>A GRCh37
NC_000014.7:g.22955206G>A NCBI36
NG_007884.1:g.24505C>T , LRG_384:g.24505C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4800C>T (MYH7) MANE Select ENSP00000347507.3:p.Ser1600=
ENST00000355349.3:c.4800C>T (MYH7) ENSP00000347507.3:p.Ser1600=
NM_000257.3:c.4800C>T (MYH7) NP_000248.2:p.Ser1600=
NR_126491.1:n.418G>A (MHRT)
XM_017021340.1:c.4800C>T (MYH7) XP_016876829.1:p.Ser1600=
NM_000257.4:c.4800C>T (MYH7) MANE Select NP_000248.2:p.Ser1600=
Search 100 bp 5'
Search 100 bp 3'