Canonical Allele Identifier: CA937669907
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs1565626339

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47339622T>C , CM000673.2:g.47339622T>C GRCh38
NC_000011.9:g.47361173T>C , CM000673.1:g.47361173T>C GRCh37
NC_000011.8:g.47317749T>C NCBI36
NG_007667.1:g.18081A>G , LRG_386:g.18081A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2067+29A>G MANE Select ENSP00000442795.1:n.2067+29A>G
ENST00000256993.8:c.2067+29A>G ENSP00000256993.5:n.2067+29A>G
ENST00000399249.6:c.2067+29A>G ENSP00000382193.2:n.2067+29A>G
ENST00000544791.1:c.2067+29A>G ENSP00000444259.1:n.2067+29A>G
ENST00000545968.5:c.2067+29A>G ENSP00000442795.1:n.2067+29A>G
NM_000256.3:c.2067+29A>G , LRG_386t1:c.2067+29A>G MANE Select NP_000247.2:n.2067+29A>G
XM_011520117.1:c.2049+29A>G XP_011518419.1:n.2049+29A>G
XM_011520118.1:c.2067+29A>G XP_011518420.1:n.2067+29A>G