Canonical Allele Identifier: CA474216980
Gene: MYBPC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.47360111A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47338560A>T , CM000673.2:g.47338560A>T GRCh38
NC_000011.9:g.47360111A>T , CM000673.1:g.47360111A>T GRCh37
NC_000011.8:g.47316687A>T NCBI36
NG_007667.1:g.19143T>A , LRG_386:g.19143T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.2268T>A MANE Select ENSP00000442795.1:p.Pro756=
ENST00000256993.8:c.2268T>A ENSP00000256993.5:p.Pro756=
ENST00000399249.6:c.2268T>A ENSP00000382193.2:p.Pro756=
ENST00000544791.1:c.2268T>A ENSP00000444259.1:p.Pro756=
ENST00000545968.5:c.2268T>A ENSP00000442795.1:p.Pro756=
NM_000256.3:c.2268T>A , LRG_386t1:c.2268T>A MANE Select NP_000247.2:p.Pro756=
XM_011520117.1:c.2250T>A XP_011518419.1:p.Pro750=
XM_011520118.1:c.2187T>A XP_011518420.1:p.Pro729=