Canonical Allele Identifier: CA474428883
Gene: MYBPC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.47354120G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47332569G>C , CM000673.2:g.47332569G>C GRCh38
NC_000011.9:g.47354120G>C , CM000673.1:g.47354120G>C GRCh37
NC_000011.8:g.47310696G>C NCBI36
NG_007667.1:g.25134C>G , LRG_386:g.25134C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3624C>G MANE Select ENSP00000442795.1:p.Pro1208=
ENST00000256993.8:c.3624C>G ENSP00000256993.5:p.Pro1208=
ENST00000399249.6:c.3624C>G ENSP00000382193.2:p.Pro1208=
ENST00000545968.5:c.3624C>G ENSP00000442795.1:p.Pro1208=
NM_000256.3:c.3624C>G , LRG_386t1:c.3624C>G MANE Select NP_000247.2:p.Pro1208=
XM_011520117.1:c.3606C>G XP_011518419.1:p.Pro1202=
XM_011520118.1:c.3543C>G XP_011518420.1:p.Pro1181=
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