Canonical Allele Identifier: CA676995816
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs1180663534

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338203C>A , CM000673.2:g.47338203C>A GRCh38
NC_000011.9:g.47359754C>A , CM000673.1:g.47359754C>A GRCh37
NC_000011.8:g.47316330C>A NCBI36
NG_007667.1:g.19500G>T , LRG_386:g.19500G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.2308+317G>T MANE Select ENSP00000442795.1:n.2308+317G>T
ENST00000256993.8:c.2308+317G>T ENSP00000256993.5:n.2308+317G>T
ENST00000399249.6:c.2308+317G>T ENSP00000382193.2:n.2308+317G>T
ENST00000544791.1:c.2308+317G>T ENSP00000444259.1:n.2308+317G>T
ENST00000545968.5:c.2308+317G>T ENSP00000442795.1:n.2308+317G>T
NM_000256.3:c.2308+317G>T , LRG_386t1:c.2308+317G>T MANE Select NP_000247.2:n.2308+317G>T
XM_011520117.1:c.2290+317G>T XP_011518419.1:n.2290+317G>T
XM_011520118.1:c.2227+317G>T XP_011518420.1:n.2227+317G>T