Canonical Allele Identifier: CA485766114
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1840632431
MyVariant Identifiers: chr14:g.23884336C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415127C>T , CM000676.2:g.23415127C>T GRCh38
NC_000014.8:g.23884336C>T , CM000676.1:g.23884336C>T GRCh37
NC_000014.7:g.22954176C>T NCBI36
NG_007884.1:g.25535G>A , LRG_384:g.25535G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.5427G>A MANE Select ENSP00000347507.3:p.Lys1809=
ENST00000355349.3:c.5427G>A ENSP00000347507.3:p.Lys1809=
NM_000257.3:c.5427G>A NP_000248.2:p.Lys1809=
XM_017021340.1:c.5427G>A XP_016876829.1:p.Lys1809=
NM_000257.4:c.5427G>A MANE Select NP_000248.2:p.Lys1809=