Canonical Allele Identifier: CA389037122
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI

Linked Data

ClinVar Variation Id: 1387798
ClinVar RCV Id: RCV001884240
dbSNP Id: rs2138640581
MyVariant Identifiers: chr14:g.23884974A>T (hg19) chr14:g.23415765A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415765A>T , CM000676.2:g.23415765A>T GRCh38
NC_000014.8:g.23884974A>T , CM000676.1:g.23884974A>T GRCh37
NC_000014.7:g.22954814A>T NCBI36
NG_007884.1:g.24897T>A , LRG_384:g.24897T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5021T>A (MYH7) MANE Select ENSP00000347507.3:p.Val1674Glu
ENST00000355349.3:c.5021T>A (MYH7) ENSP00000347507.3:p.Val1674Glu
NM_000257.3:c.5021T>A (MYH7) NP_000248.2:p.Val1674Glu
NR_126491.1:n.197A>T (MHRT)
XM_017021340.1:c.5021T>A (MYH7) XP_016876829.1:p.Val1674Glu
NM_000257.4:c.5021T>A (MYH7) MANE Select NP_000248.2:p.Val1674Glu
Search 100 bp 5'
Search 100 bp 3'