Canonical Allele Identifier: CA474220934
Gene: MYBPC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.47367858T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47346307T>A , CM000673.2:g.47346307T>A GRCh38
NC_000011.9:g.47367858T>A , CM000673.1:g.47367858T>A GRCh37
NC_000011.8:g.47324434T>A NCBI36
NG_007667.1:g.11396A>T , LRG_386:g.11396A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.990A>T MANE Select ENSP00000442795.1:p.Pro330=
ENST00000256993.8:c.990A>T ENSP00000256993.5:p.Pro330=
ENST00000399249.6:c.990A>T ENSP00000382193.2:p.Pro330=
ENST00000544791.1:c.990A>T ENSP00000444259.1:p.Pro330=
ENST00000545968.5:c.990A>T ENSP00000442795.1:p.Pro330=
NM_000256.3:c.990A>T , LRG_386t1:c.990A>T MANE Select NP_000247.2:p.Pro330=
XM_011520117.1:c.972A>T XP_011518419.1:p.Pro324=
XM_011520118.1:c.990A>T XP_011518420.1:p.Pro330=