Canonical Allele Identifier: CA10603214
Gene: MYBPC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 279971
ClinVar RCV Id: RCV001385587
dbSNP Id: rs587776700
MyVariant Identifiers: chr11:g.47368581C>T (hg19) chr11:g.47347030C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47347030C>T , CM000673.2:g.47347030C>T GRCh38
NC_000011.9:g.47368581C>T , CM000673.1:g.47368581C>T GRCh37
NC_000011.8:g.47325157C>T NCBI36
NG_007667.1:g.10673G>A , LRG_386:g.10673G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.906-1G>A MANE Select ENSP00000442795.1:n.906-1G>A
ENST00000256993.8:c.906-383G>A ENSP00000256993.5:n.906-383G>A
ENST00000399249.6:c.906-383G>A ENSP00000382193.2:n.906-383G>A
ENST00000544791.1:c.906-1G>A ENSP00000444259.1:n.906-1G>A
ENST00000545968.5:c.906-1G>A ENSP00000442795.1:n.906-1G>A
NM_000256.3:c.906-1G>A , LRG_386t1:c.906-1G>A MANE Select NP_000247.2:n.906-1G>A
XM_011520117.1:c.906-1G>A XP_011518419.1:n.906-1G>A
XM_011520118.1:c.906-1G>A XP_011518420.1:n.906-1G>A
Search 100 bp 5'
Search 100 bp 3'