Canonical Allele Identifier: CA2123458014
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892663486
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23425628G>T , CM000676.2:g.23425628G>T GRCh38
NC_000014.8:g.23894837G>T , CM000676.1:g.23894837G>T GRCh37
NC_000014.7:g.22964677G>T NCBI36
NG_007884.1:g.15034C>A , LRG_384:g.15034C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2286+67C>A MANE Select ENSP00000347507.3:n.2286+67C>A
ENST00000355349.3:c.2286+67C>A ENSP00000347507.3:n.2286+67C>A
NM_000257.3:c.2286+67C>A NP_000248.2:n.2286+67C>A
XR_245686.3:n.2392+67C>A
XM_017021340.1:c.2286+67C>A XP_016876829.1:n.2286+67C>A
NM_000257.4:c.2286+67C>A MANE Select NP_000248.2:n.2286+67C>A
Search 100 bp 5'
Search 100 bp 3'