Canonical Allele Identifier: CA474429269
Gene: MYBPC3 HGNC NCBI

Linked Data

gnomAD v4: 11-47333690-C-A
MyVariant Identifiers: chr11:g.47355241C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47333690C>A , CM000673.2:g.47333690C>A GRCh38
NC_000011.9:g.47355241C>A , CM000673.1:g.47355241C>A GRCh37
NC_000011.8:g.47311817C>A NCBI36
NG_007667.1:g.24013G>T , LRG_386:g.24013G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000545968.6:c.3057G>T MANE Select ENSP00000442795.1:p.Val1019=
ENST00000256993.8:c.3057G>T ENSP00000256993.5:p.Val1019=
ENST00000399249.6:c.3057G>T ENSP00000382193.2:p.Val1019=
ENST00000545968.5:c.3057G>T ENSP00000442795.1:p.Val1019=
NM_000256.3:c.3057G>T , LRG_386t1:c.3057G>T MANE Select NP_000247.2:p.Val1019=
XM_011520117.1:c.3039G>T XP_011518419.1:p.Val1013=
XM_011520118.1:c.2976G>T XP_011518420.1:p.Val992=
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