Canonical Allele Identifier: CA2123450190
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422031G= , CM000676.2:g.23422031G= GRCh38
NC_000014.8:g.23891240G= , CM000676.1:g.23891240G= GRCh37
NC_000014.7:g.22961080G= NCBI36
NG_007884.1:g.18631C= , LRG_384:g.18631C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+149C= MANE Select ENSP00000347507.3:n.3245+149C=
ENST00000355349.3:c.3245+149C= ENSP00000347507.3:n.3245+149C=
NM_000257.3:c.3245+149C= NP_000248.2:n.3245+149C=
XR_245686.3:n.3351+149C=
XM_017021340.1:c.3245+149C= XP_016876829.1:n.3245+149C=
NM_000257.4:c.3245+149C= MANE Select NP_000248.2:n.3245+149C=