Canonical Allele Identifier: CA389046724
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23893159G>C (hg19) chr14:g.23423950G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423950G>C , CM000676.2:g.23423950G>C GRCh38
NC_000014.8:g.23893159G>C , CM000676.1:g.23893159G>C GRCh37
NC_000014.7:g.22962999G>C NCBI36
NG_007884.1:g.16712C>G , LRG_384:g.16712C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.2879C>G MANE Select ENSP00000347507.3:p.Thr960Arg
ENST00000355349.3:c.2879C>G ENSP00000347507.3:p.Thr960Arg
NM_000257.3:c.2879C>G NP_000248.2:p.Thr960Arg
XR_245686.3:n.2985C>G
XM_017021340.1:c.2879C>G XP_016876829.1:p.Thr960Arg
NM_000257.4:c.2879C>G MANE Select NP_000248.2:p.Thr960Arg
Search 100 bp 5'
Search 100 bp 3'