Canonical Allele Identifier: CA2123453666
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423803T= , CM000676.2:g.23423803T= GRCh38
NC_000014.8:g.23893012T= , CM000676.1:g.23893012T= GRCh37
NC_000014.7:g.22962852T= NCBI36
NG_007884.1:g.16859A= , LRG_384:g.16859A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2923-80A= MANE Select ENSP00000347507.3:n.2923-80A=
ENST00000355349.3:c.2923-80A= ENSP00000347507.3:n.2923-80A=
NM_000257.3:c.2923-80A= NP_000248.2:n.2923-80A=
XR_245686.3:n.3029-80A=
XM_017021340.1:c.2923-80A= XP_016876829.1:n.2923-80A=
NM_000257.4:c.2923-80A= MANE Select NP_000248.2:n.2923-80A=