Canonical Allele Identifier: CA079275
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 922548
dbSNP Id: rs769925144

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47333225T>A , CM000673.2:g.47333225T>A GRCh38
NC_000011.9:g.47354776T>A , CM000673.1:g.47354776T>A GRCh37
NC_000011.8:g.47311352T>A NCBI36
NG_007667.1:g.24478A>T , LRG_386:g.24478A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3299A>T MANE Select ENSP00000442795.1:p.Tyr1100Phe
ENST00000256993.8:c.3299A>T ENSP00000256993.5:p.Tyr1100Phe
ENST00000399249.6:c.3299A>T ENSP00000382193.2:p.Tyr1100Phe
ENST00000545968.5:c.3299A>T ENSP00000442795.1:p.Tyr1100Phe
NM_000256.3:c.3299A>T , LRG_386t1:c.3299A>T MANE Select NP_000247.2:p.Tyr1100Phe
XM_011520117.1:c.3281A>T XP_011518419.1:p.Tyr1094Phe
XM_011520118.1:c.3218A>T XP_011518420.1:p.Tyr1073Phe