Canonical Allele Identifier: CA474429819
Gene: MYBPC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.47372983T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47351432T>G , CM000673.2:g.47351432T>G GRCh38
NC_000011.9:g.47372983T>G , CM000673.1:g.47372983T>G GRCh37
NC_000011.8:g.47329559T>G NCBI36
NG_007667.1:g.6271A>C , LRG_386:g.6271A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.99A>C MANE Select ENSP00000442795.1:p.Thr33=
ENST00000256993.8:c.99A>C ENSP00000256993.5:p.Thr33=
ENST00000399249.6:c.99A>C ENSP00000382193.2:p.Thr33=
ENST00000544791.1:c.99A>C ENSP00000444259.1:p.Thr33=
ENST00000545968.5:c.99A>C ENSP00000442795.1:p.Thr33=
NM_000256.3:c.99A>C , LRG_386t1:c.99A>C MANE Select NP_000247.2:p.Thr33=
XM_011520117.1:c.99A>C XP_011518419.1:p.Thr33=
XM_011520118.1:c.99A>C XP_011518420.1:p.Thr33=