Canonical Allele Identifier: CA044154

Linked Data

ClinVar Variation Id: 853296
ClinVar RCV Id: RCV001058079
dbSNP Id: rs762272480

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416060T>C , CM000676.2:g.23416060T>C GRCh38
NC_000014.8:g.23885269T>C , CM000676.1:g.23885269T>C GRCh37
NC_000014.7:g.22955109T>C NCBI36
NG_007884.1:g.24602A>G , LRG_384:g.24602A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4897A>G (MYH7) MANE Select ENSP00000347507.3:p.Asn1633Asp
ENST00000355349.3:c.4897A>G (MYH7) ENSP00000347507.3:p.Asn1633Asp
NM_000257.3:c.4897A>G (MYH7) NP_000248.2:p.Asn1633Asp
NR_126491.1:n.321T>C (MHRT)
XM_017021340.1:c.4897A>G (MYH7) XP_016876829.1:p.Asn1633Asp
NM_000257.4:c.4897A>G (MYH7) MANE Select NP_000248.2:p.Asn1633Asp