Canonical Allele Identifier: CA389049783
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23896880A>C (hg19) chr14:g.23427671A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23427671A>C , CM000676.2:g.23427671A>C GRCh38
NC_000014.8:g.23896880A>C , CM000676.1:g.23896880A>C GRCh37
NC_000014.7:g.22966720A>C NCBI36
NG_007884.1:g.12991T>G , LRG_384:g.12991T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1802T>G MANE Select ENSP00000347507.3:p.Leu601Arg
ENST00000355349.3:c.1802T>G ENSP00000347507.3:p.Leu601Arg
NM_000257.3:c.1802T>G NP_000248.2:p.Leu601Arg
XR_245686.3:n.1908T>G
XM_017021340.1:c.1802T>G XP_016876829.1:p.Leu601Arg
NM_000257.4:c.1802T>G MANE Select NP_000248.2:p.Leu601Arg
Search 100 bp 5'
Search 100 bp 3'