Canonical Allele Identifier: CA389051125
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 525009
ClinVar RCV Id: RCV000628968
dbSNP Id: rs1555338370
MyVariant Identifiers: chr14:g.23898490G>T (hg19) chr14:g.23429281G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429281G>T , CM000676.2:g.23429281G>T GRCh38
NC_000014.8:g.23898490G>T , CM000676.1:g.23898490G>T GRCh37
NC_000014.7:g.22968330G>T NCBI36
NG_007884.1:g.11381C>A , LRG_384:g.11381C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1205C>A MANE Select ENSP00000347507.3:p.Pro402His
ENST00000355349.3:c.1205C>A ENSP00000347507.3:p.Pro402His
NM_000257.3:c.1205C>A NP_000248.2:p.Pro402His
XR_245686.3:n.1311C>A
XM_017021340.1:c.1205C>A XP_016876829.1:p.Pro402His
NM_000257.4:c.1205C>A MANE Select NP_000248.2:p.Pro402His
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