Canonical Allele Identifier: CA485766444

Linked Data

ClinVar Variation Id: 1560463
ClinVar RCV Id: RCV002197798
dbSNP Id: rs2138642484
MyVariant Identifiers: chr14:g.23885480C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416271C>T , CM000676.2:g.23416271C>T GRCh38
NC_000014.8:g.23885480C>T , CM000676.1:g.23885480C>T GRCh37
NC_000014.7:g.22955320C>T NCBI36
NG_007884.1:g.24391G>A , LRG_384:g.24391G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4686G>A (MYH7) MANE Select ENSP00000347507.3:p.Gln1562=
ENST00000355349.3:c.4686G>A (MYH7) ENSP00000347507.3:p.Gln1562=
NM_000257.3:c.4686G>A (MYH7) NP_000248.2:p.Gln1562=
NR_126491.1:n.532C>T (MHRT)
XM_017021340.1:c.4686G>A (MYH7) XP_016876829.1:p.Gln1562=
NM_000257.4:c.4686G>A (MYH7) MANE Select NP_000248.2:p.Gln1562=