Canonical Allele Identifier: CA2123455233
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424486T= , CM000676.2:g.23424486T= GRCh38
NC_000014.8:g.23893695T= , CM000676.1:g.23893695T= GRCh37
NC_000014.7:g.22963535T= NCBI36
NG_007884.1:g.16176A= , LRG_384:g.16176A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2679+283A= MANE Select ENSP00000347507.3:n.2679+283A=
ENST00000355349.3:c.2679+283A= ENSP00000347507.3:n.2679+283A=
NM_000257.3:c.2679+283A= NP_000248.2:n.2679+283A=
XR_245686.3:n.2785+283A=
XM_017021340.1:c.2679+283A= XP_016876829.1:n.2679+283A=
NM_000257.4:c.2679+283A= MANE Select NP_000248.2:n.2679+283A=