Canonical Allele Identifier: CA1969331871
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs2095884611

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338243G>C , CM000673.2:g.47338243G>C GRCh38
NC_000011.9:g.47359794G>C , CM000673.1:g.47359794G>C GRCh37
NC_000011.8:g.47316370G>C NCBI36
NG_007667.1:g.19460C>G , LRG_386:g.19460C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2308+277C>G MANE Select ENSP00000442795.1:n.2308+277C>G
ENST00000256993.8:c.2308+277C>G ENSP00000256993.5:n.2308+277C>G
ENST00000399249.6:c.2308+277C>G ENSP00000382193.2:n.2308+277C>G
ENST00000544791.1:c.2308+277C>G ENSP00000444259.1:n.2308+277C>G
ENST00000545968.5:c.2308+277C>G ENSP00000442795.1:n.2308+277C>G
NM_000256.3:c.2308+277C>G , LRG_386t1:c.2308+277C>G MANE Select NP_000247.2:n.2308+277C>G
XM_011520117.1:c.2290+277C>G XP_011518419.1:n.2290+277C>G
XM_011520118.1:c.2227+277C>G XP_011518420.1:n.2227+277C>G