Canonical Allele Identifier: CA079539
Gene: MYBPC3 HGNC NCBI

Linked Data

dbSNP Id: rs746042492
ExAC: 11:47353660 C / G
gnomAD v2: 11-47353660-C-G
gnomAD v4: 11-47332109-C-G
MyVariant Identifiers: chr11:g.47353660C>G (hg19) chr11:g.47353660_47353661delinsGT (hg19) chr11:g.47332109C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47332109C>G , CM000673.2:g.47332109C>G GRCh38
NC_000011.9:g.47353660C>G , CM000673.1:g.47353660C>G GRCh37
NC_000011.8:g.47310236C>G NCBI36
NG_007667.1:g.25594G>C , LRG_386:g.25594G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000545968.6:c.3777G>C MANE Select ENSP00000442795.1:p.Gln1259His
ENST00000256993.8:c.3777G>C ENSP00000256993.5:p.Gln1259His
ENST00000399249.6:c.3777G>C ENSP00000382193.2:p.Gln1259His
ENST00000545968.5:c.3777G>C ENSP00000442795.1:p.Gln1259His
NM_000256.3:c.3777G>C , LRG_386t1:c.3777G>C MANE Select NP_000247.2:p.Gln1259His
XM_011520117.1:c.3759G>C XP_011518419.1:p.Gln1253His
XM_011520118.1:c.3696G>C XP_011518420.1:p.Gln1232His
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