Canonical Allele Identifier: CA389040150

Linked Data

ClinVar Variation Id: 954891
ClinVar RCV Id: RCV001227427
dbSNP Id: rs1489767429

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417549T>C , CM000676.2:g.23417549T>C GRCh38
NC_000014.8:g.23886758T>C , CM000676.1:g.23886758T>C GRCh37
NC_000014.7:g.22956598T>C NCBI36
NG_007884.1:g.23113A>G , LRG_384:g.23113A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4307A>G (MYH7) MANE Select ENSP00000347507.3:p.Asn1436Ser
ENST00000355349.3:c.4307A>G (MYH7) ENSP00000347507.3:p.Asn1436Ser
NM_000257.3:c.4307A>G (MYH7) NP_000248.2:p.Asn1436Ser
NR_126491.1:n.830T>C (MHRT)
XM_017021340.1:c.4307A>G (MYH7) XP_016876829.1:p.Asn1436Ser
NM_000257.4:c.4307A>G (MYH7) MANE Select NP_000248.2:p.Asn1436Ser