Canonical Allele Identifier: CA2624251164
Gene: MYH7 HGNC NCBI

Linked Data

gnomAD v4: 14-23431494-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431494A>T , CM000676.2:g.23431494A>T GRCh38
NC_000014.8:g.23900703A>T , CM000676.1:g.23900703A>T GRCh37
NC_000014.7:g.22970543A>T NCBI36
NG_007884.1:g.9168T>A , LRG_384:g.9168T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.733-13T>A MANE Select ENSP00000347507.3:n.733-13T>A
ENST00000355349.3:c.733-13T>A ENSP00000347507.3:n.733-13T>A
NM_000257.3:c.733-13T>A NP_000248.2:n.733-13T>A
XR_245686.3:n.839-13T>A
XM_017021340.1:c.733-13T>A XP_016876829.1:n.733-13T>A
NM_000257.4:c.733-13T>A MANE Select NP_000248.2:n.733-13T>A
Search 100 bp 5'
Search 100 bp 3'