Canonical Allele Identifier: CA474428827
Gene: MYBPC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.47353651T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47332100T>C , CM000673.2:g.47332100T>C GRCh38
NC_000011.9:g.47353651T>C , CM000673.1:g.47353651T>C GRCh37
NC_000011.8:g.47310227T>C NCBI36
NG_007667.1:g.25603A>G , LRG_386:g.25603A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.3786A>G MANE Select ENSP00000442795.1:p.Ala1262=
ENST00000256993.8:c.3786A>G ENSP00000256993.5:p.Ala1262=
ENST00000399249.6:c.3786A>G ENSP00000382193.2:p.Ala1262=
ENST00000545968.5:c.3786A>G ENSP00000442795.1:p.Ala1262=
NM_000256.3:c.3786A>G , LRG_386t1:c.3786A>G MANE Select NP_000247.2:p.Ala1262=
XM_011520117.1:c.3768A>G XP_011518419.1:p.Ala1256=
XM_011520118.1:c.3705A>G XP_011518420.1:p.Ala1235=
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