Canonical Allele Identifier: CA485766504

Linked Data

ClinVar Variation Id: 2448062
ClinVar RCV Id: RCV003168158
MyVariant Identifiers: chr14:g.23885303G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416094G>A , CM000676.2:g.23416094G>A GRCh38
NC_000014.8:g.23885303G>A , CM000676.1:g.23885303G>A GRCh37
NC_000014.7:g.22955143G>A NCBI36
NG_007884.1:g.24568C>T , LRG_384:g.24568C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4863C>T (MYH7) MANE Select ENSP00000347507.3:p.Asp1621=
ENST00000355349.3:c.4863C>T (MYH7) ENSP00000347507.3:p.Asp1621=
NM_000257.3:c.4863C>T (MYH7) NP_000248.2:p.Asp1621=
NR_126491.1:n.355G>A (MHRT)
XM_017021340.1:c.4863C>T (MYH7) XP_016876829.1:p.Asp1621=
NM_000257.4:c.4863C>T (MYH7) MANE Select NP_000248.2:p.Asp1621=