Canonical Allele Identifier: CA2123448156
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420728C= , CM000676.2:g.23420728C= GRCh38
NC_000014.8:g.23889937C= , CM000676.1:g.23889937C= GRCh37
NC_000014.7:g.22959777C= NCBI36
NG_007884.1:g.19934G= , LRG_384:g.19934G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+230G= MANE Select ENSP00000347507.3:n.3336+230G=
ENST00000355349.3:c.3336+230G= ENSP00000347507.3:n.3336+230G=
NM_000257.3:c.3336+230G= NP_000248.2:n.3336+230G=
XR_245686.3:n.3444+230G=
XM_017021340.1:c.3336+230G= XP_016876829.1:n.3336+230G=
NM_000257.4:c.3336+230G= MANE Select NP_000248.2:n.3336+230G=