Canonical Allele Identifier: CA2671465799
Gene: BMPR1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95154882_95154883dup , CM000666.2:g.95154882_95154883dup GRCh38
NC_000004.11:g.96076033_96076034dup , CM000666.1:g.96076033_96076034dup GRCh37
NC_000004.10:g.96295056_96295057dup NCBI36
NG_009245.1:g.401906_401907dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000440890.7:c.*209_*210dup ENSP00000401907.2:n.*209_*210dup
ENST00000509540.6:c.*13+196_*13+197dup ENSP00000421671.1:n.*13+196_*13+197dup
ENST00000515059.6:c.*209_*210dup MANE Select ENSP00000426617.1:n.*209_*210dup
ENST00000672698.1:c.*209_*210dup ENSP00000500035.1:n.*209_*210dup
ENST00000394931.1:c.*209_*210dup ENSP00000378389.1:n.*209_*210dup
ENST00000440890.6:c.*209_*210dup ENSP00000401907.2:n.*209_*210dup
ENST00000515059.5:c.*209_*210dup ENSP00000426617.1:n.*209_*210dup
NM_001203.2:c.*209_*210dup NP_001194.1:n.*209_*210dup
NM_001256792.1:c.*209_*210dup NP_001243721.1:n.*209_*210dup
NM_001256793.1:c.*209_*210dup NP_001243722.1:n.*209_*210dup
NM_001256794.1:c.*209_*210dup NP_001243723.1:n.*209_*210dup
XM_011532201.1:c.*209_*210dup XP_011530503.1:n.*209_*210dup
XM_011532202.1:c.*209_*210dup XP_011530504.1:n.*209_*210dup
XM_011532201.2:c.*209_*210dup XP_011530503.1:n.*209_*210dup
XM_017008558.1:c.*209_*210dup XP_016864047.1:n.*209_*210dup
XM_017008559.1:c.*209_*210dup XP_016864048.1:n.*209_*210dup
XM_017008560.1:c.*209_*210dup XP_016864049.1:n.*209_*210dup
XM_017008561.1:c.*209_*210dup XP_016864050.1:n.*209_*210dup
NM_001203.3:c.*209_*210dup MANE Select NP_001194.1:n.*209_*210dup
NM_001256793.2:c.*209_*210dup NP_001243722.1:n.*209_*210dup
NM_001256792.2:c.*209_*210dup NP_001243721.1:n.*209_*210dup