Canonical Allele Identifier: CA916754563
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1559070335

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202542615del , CM000664.2:g.202542615del GRCh38
NC_000002.11:g.203407338del , CM000664.1:g.203407338del GRCh37
NC_000002.10:g.203115583del NCBI36
NG_009363.1:g.171289del , LRG_712:g.171289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1413+168del MANE Select ENSP00000363708.4:n.1413+168del
ENST00000638587.1:c.1344+168del ENSP00000491062.1:n.1344+168del
ENST00000374574.2:c.1413+168del ENSP00000363702.2:n.1413+168del
ENST00000374580.8:c.1413+168del ENSP00000363708.4:n.1413+168del
NM_001204.6:c.1413+168del , LRG_712t1:c.1413+168del NP_001195.2:n.1413+168del
XM_011511687.1:c.1413+168del XP_011509989.1:n.1413+168del
XM_011511688.1:c.1413+168del XP_011509990.1:n.1413+168del
NM_001204.7:c.1413+168del MANE Select NP_001195.2:n.1413+168del