Canonical Allele Identifier: CA010144
Community Standard Title: NM_000256.3(MYBPC3):c.1351+2T>C
Gene: MYBPC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47343019A>G , CM000673.2:g.47343019A>G GRCh38
NC_000011.9:g.47364570A>G , CM000673.1:g.47364570A>G GRCh37
NC_000011.8:g.47321146A>G NCBI36
NG_007667.1:g.14684T>C , LRG_386:g.14684T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000256.3:c.1351+2T>C , LRG_386t1:c.1351+2T>C MANE Select NP_000247.2:n.1351+2T>C
ENST00000545968.6:c.1351+2T>C MANE Select ENSP00000442795.1:n.1351+2T>C
ENST00000256993.8:c.1351+2T>C ENSP00000256993.5:n.1351+2T>C
ENST00000399249.6:c.1351+2T>C ENSP00000382193.2:n.1351+2T>C
ENST00000544791.1:c.1351+2T>C ENSP00000444259.1:n.1351+2T>C
ENST00000545968.5:c.1351+2T>C ENSP00000442795.1:n.1351+2T>C
XM_011520117.1:c.1333+2T>C XP_011518419.1:n.1333+2T>C
XM_011520118.1:c.1351+2T>C XP_011518420.1:n.1351+2T>C