Canonical Allele Identifier: CA677014558
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs1306474802
gnomAD v3: 11-47333034-T-C
gnomAD v4: 11-47333034-T-C
MyVariant Identifiers: chr11:g.47354585T>C (hg19) chr11:g.47333034T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47333034T>C , CM000673.2:g.47333034T>C GRCh38
NC_000011.9:g.47354585T>C , CM000673.1:g.47354585T>C GRCh37
NC_000011.8:g.47311161T>C NCBI36
NG_007667.1:g.24669A>G , LRG_386:g.24669A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3331-61A>G MANE Select ENSP00000442795.1:n.3331-61A>G
ENST00000256993.8:c.3331-61A>G ENSP00000256993.5:n.3331-61A>G
ENST00000399249.6:c.3331-61A>G ENSP00000382193.2:n.3331-61A>G
ENST00000545968.5:c.3331-61A>G ENSP00000442795.1:n.3331-61A>G
NM_000256.3:c.3331-61A>G , LRG_386t1:c.3331-61A>G MANE Select NP_000247.2:n.3331-61A>G
XM_011520117.1:c.3313-61A>G XP_011518419.1:n.3313-61A>G
XM_011520118.1:c.3250-61A>G XP_011518420.1:n.3250-61A>G
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