Canonical Allele Identifier: CA613317792
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 880735
ClinVar RCV Id: RCV001109228 RCV001109229 RCV001114872 RCV003320230 RCV003586266
dbSNP Id: rs1346778409
gnomAD v2: 14-23900957-G-A
gnomAD v3: 14-23431748-G-A
gnomAD v4: 14-23431748-G-A
MyVariant Identifiers: chr14:g.23900957G>A (hg19) chr14:g.23431748G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431748G>A , CM000676.2:g.23431748G>A GRCh38
NC_000014.8:g.23900957G>A , CM000676.1:g.23900957G>A GRCh37
NC_000014.7:g.22970797G>A NCBI36
NG_007884.1:g.8914C>T , LRG_384:g.8914C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.639+13C>T MANE Select ENSP00000347507.3:n.639+13C>T
ENST00000355349.3:c.639+13C>T ENSP00000347507.3:n.639+13C>T
NM_000257.3:c.639+13C>T NP_000248.2:n.639+13C>T
XR_245686.3:n.745+13C>T
XM_017021340.1:c.639+13C>T XP_016876829.1:n.639+13C>T
NM_000257.4:c.639+13C>T MANE Select NP_000248.2:n.639+13C>T
Search 100 bp 5'
Search 100 bp 3'