Canonical Allele Identifier: CA485766051
Gene: MYH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.23884574G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415365G>C , CM000676.2:g.23415365G>C GRCh38
NC_000014.8:g.23884574G>C , CM000676.1:g.23884574G>C GRCh37
NC_000014.7:g.22954414G>C NCBI36
NG_007884.1:g.25297C>G , LRG_384:g.25297C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5283+16C>G MANE Select ENSP00000347507.3:n.5283+16C>G
ENST00000355349.3:c.5283+16C>G ENSP00000347507.3:n.5283+16C>G
NM_000257.3:c.5283+16C>G NP_000248.2:n.5283+16C>G
XM_017021340.1:c.5283+16C>G XP_016876829.1:n.5283+16C>G
NM_000257.4:c.5283+16C>G MANE Select NP_000248.2:n.5283+16C>G
Search 100 bp 5'
Search 100 bp 3'