Canonical Allele Identifier: CA485766078
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1595072137
MyVariant Identifiers: chr14:g.23884578T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415369T>G , CM000676.2:g.23415369T>G GRCh38
NC_000014.8:g.23884578T>G , CM000676.1:g.23884578T>G GRCh37
NC_000014.7:g.22954418T>G NCBI36
NG_007884.1:g.25293A>C , LRG_384:g.25293A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5283+12A>C MANE Select ENSP00000347507.3:n.5283+12A>C
ENST00000355349.3:c.5283+12A>C ENSP00000347507.3:n.5283+12A>C
NM_000257.3:c.5283+12A>C NP_000248.2:n.5283+12A>C
XM_017021340.1:c.5283+12A>C XP_016876829.1:n.5283+12A>C
NM_000257.4:c.5283+12A>C MANE Select NP_000248.2:n.5283+12A>C
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