Canonical Allele Identifier: CA937661940
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs1595850404

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47350995T>G , CM000673.2:g.47350995T>G GRCh38
NC_000011.9:g.47372546T>G , CM000673.1:g.47372546T>G GRCh37
NC_000011.8:g.47329122T>G NCBI36
NG_007667.1:g.6708A>C , LRG_386:g.6708A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.292+244A>C MANE Select ENSP00000442795.1:n.292+244A>C
ENST00000256993.8:c.292+244A>C ENSP00000256993.5:n.292+244A>C
ENST00000399249.6:c.292+244A>C ENSP00000382193.2:n.292+244A>C
ENST00000544791.1:c.292+244A>C ENSP00000444259.1:n.292+244A>C
ENST00000545968.5:c.292+244A>C ENSP00000442795.1:n.292+244A>C
NM_000256.3:c.292+244A>C , LRG_386t1:c.292+244A>C MANE Select NP_000247.2:n.292+244A>C
XM_011520117.1:c.292+244A>C XP_011518419.1:n.292+244A>C
XM_011520118.1:c.292+244A>C XP_011518420.1:n.292+244A>C