Canonical Allele Identifier: CA389045792
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423601G>C , CM000676.2:g.23423601G>C GRCh38
NC_000014.8:g.23892810G>C , CM000676.1:g.23892810G>C GRCh37
NC_000014.7:g.22962650G>C NCBI36
NG_007884.1:g.17061C>G , LRG_384:g.17061C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3045C>G MANE Select ENSP00000347507.3:p.Asp1015Glu
ENST00000355349.3:c.3045C>G ENSP00000347507.3:p.Asp1015Glu
NM_000257.3:c.3045C>G NP_000248.2:p.Asp1015Glu
XR_245686.3:n.3151C>G
XM_017021340.1:c.3045C>G XP_016876829.1:p.Asp1015Glu
NM_000257.4:c.3045C>G MANE Select NP_000248.2:p.Asp1015Glu