Canonical Allele Identifier: CA2123446661
Gene: MYH7 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23429609G= , CM000676.2:g.23429609G= GRCh38
NC_000014.8:g.23898818G= , CM000676.1:g.23898818G= GRCh37
NC_000014.7:g.22968658G= NCBI36
NG_007884.1:g.11053C= , LRG_384:g.11053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.1138+166C= MANE Select ENSP00000347507.3:n.1138+166C=
ENST00000355349.3:c.1138+166C= ENSP00000347507.3:n.1138+166C=
NM_000257.3:c.1138+166C= NP_000248.2:n.1138+166C=
XR_245686.3:n.1244+166C=
XM_017021340.1:c.1138+166C= XP_016876829.1:n.1138+166C=
NM_000257.4:c.1138+166C= MANE Select NP_000248.2:n.1138+166C=
Search 100 bp 5'
Search 100 bp 3'