Canonical Allele Identifier: CA485766506

Linked Data

ClinVar Variation Id: 1549277
dbSNP Id: rs1595073316
MyVariant Identifiers: chr14:g.23885306T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416097T>C , CM000676.2:g.23416097T>C GRCh38
NC_000014.8:g.23885306T>C , CM000676.1:g.23885306T>C GRCh37
NC_000014.7:g.22955146T>C NCBI36
NG_007884.1:g.24565A>G , LRG_384:g.24565A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4860A>G (MYH7) MANE Select ENSP00000347507.3:p.Gly1620=
ENST00000355349.3:c.4860A>G (MYH7) ENSP00000347507.3:p.Gly1620=
NM_000257.3:c.4860A>G (MYH7) NP_000248.2:p.Gly1620=
NR_126491.1:n.358T>C (MHRT)
XM_017021340.1:c.4860A>G (MYH7) XP_016876829.1:p.Gly1620=
NM_000257.4:c.4860A>G (MYH7) MANE Select NP_000248.2:p.Gly1620=