Canonical Allele Identifier: CA389043902
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23889346T>G (hg19) chr14:g.23420137T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420137T>G , CM000676.2:g.23420137T>G GRCh38
NC_000014.8:g.23889346T>G , CM000676.1:g.23889346T>G GRCh37
NC_000014.7:g.22959186T>G NCBI36
NG_007884.1:g.20525A>C , LRG_384:g.20525A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3434A>C MANE Select ENSP00000347507.3:p.Glu1145Ala
ENST00000355349.3:c.3434A>C ENSP00000347507.3:p.Glu1145Ala
NM_000257.3:c.3434A>C NP_000248.2:p.Glu1145Ala
XM_017021340.1:c.3434A>C XP_016876829.1:p.Glu1145Ala
NM_000257.4:c.3434A>C MANE Select NP_000248.2:p.Glu1145Ala
Search 100 bp 5'
Search 100 bp 3'