Canonical Allele Identifier: CA478842079
Gene: PRB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.11421042G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11268108G>T , CM000674.2:g.11268108G>T GRCh38
NC_000012.11:g.11421042G>T , CM000674.1:g.11421042G>T GRCh37
NC_000012.10:g.11312309G>T NCBI36
NG_013305.2:g.6600C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000538488.3:c.141C>A MANE Select ENSP00000442626.2:p.Pro47=
ENST00000381842.7:c.141C>A ENSP00000371264.3:p.Pro47=
ENST00000538488.2:c.141C>A ENSP00000442626.2:p.Pro47=
ENST00000539835.1:n.148C>A
NM_006249.5:c.141C>A NP_006240.4:p.Pro47=
NM_001394862.1:c.141C>A MANE Select NP_001381791.1:p.Pro47=
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