Canonical Allele Identifier: CA16619334
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 419467
ClinVar RCV Id: RCV001321874
dbSNP Id: rs1064793891

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47333336G>C , CM000673.2:g.47333336G>C GRCh38
NC_000011.9:g.47354887G>C , CM000673.1:g.47354887G>C GRCh37
NC_000011.8:g.47311463G>C NCBI36
NG_007667.1:g.24367C>G , LRG_386:g.24367C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.3191-3C>G MANE Select ENSP00000442795.1:n.3191-3C>G
ENST00000256993.8:c.3191-3C>G ENSP00000256993.5:n.3191-3C>G
ENST00000399249.6:c.3191-3C>G ENSP00000382193.2:n.3191-3C>G
ENST00000545968.5:c.3191-3C>G ENSP00000442795.1:n.3191-3C>G
NM_000256.3:c.3191-3C>G , LRG_386t1:c.3191-3C>G MANE Select NP_000247.2:n.3191-3C>G
XM_011520117.1:c.3173-3C>G XP_011518419.1:n.3173-3C>G
XM_011520118.1:c.3110-3C>G XP_011518420.1:n.3110-3C>G