Canonical Allele Identifier: CA389041000
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23418300A>C , CM000676.2:g.23418300A>C GRCh38
NC_000014.8:g.23887509A>C , CM000676.1:g.23887509A>C GRCh37
NC_000014.7:g.22957349A>C NCBI36
NG_007884.1:g.22362T>G , LRG_384:g.22362T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4079T>G MANE Select ENSP00000347507.3:p.Val1360Gly
ENST00000355349.3:c.4079T>G ENSP00000347507.3:p.Val1360Gly
NM_000257.3:c.4079T>G NP_000248.2:p.Val1360Gly
XM_017021340.1:c.4079T>G XP_016876829.1:p.Val1360Gly
NM_000257.4:c.4079T>G MANE Select NP_000248.2:p.Val1360Gly