Canonical Allele Identifier: CA1321507357
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1692284996

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464757_202464759del , CM000664.2:g.202464757_202464759del GRCh38
NC_000002.11:g.203329480_203329482del , CM000664.1:g.203329480_203329482del GRCh37
NC_000002.10:g.203037725_203037727del NCBI36
NG_009363.1:g.93431_93433del , LRG_712:g.93431_93433del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.77-52_77-50del MANE Select ENSP00000363708.4:n.77-52_77-50del
ENST00000374574.2:c.77-52_77-50del ENSP00000363702.2:n.77-52_77-50del
ENST00000374580.8:c.77-52_77-50del ENSP00000363708.4:n.77-52_77-50del
NM_001204.6:c.77-52_77-50del , LRG_712t1:c.77-52_77-50del NP_001195.2:n.77-52_77-50del
XM_011511687.1:c.77-52_77-50del XP_011509989.1:n.77-52_77-50del
XM_011511688.1:c.77-52_77-50del XP_011509990.1:n.77-52_77-50del
NM_001204.7:c.77-52_77-50del MANE Select NP_001195.2:n.77-52_77-50del