Canonical Allele Identifier: CA645532629
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs2106006908

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202518897del , CM000664.2:g.202518897del GRCh38
NC_000002.11:g.203383620del , CM000664.1:g.203383620del GRCh37
NC_000002.10:g.203091865del NCBI36
NG_009363.1:g.147571del , LRG_712:g.147571del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.697del MANE Select ENSP00000363708.4:p.Ser233ProfsTer19
ENST00000638587.1:c.628del ENSP00000491062.1:p.Ser210ProfsTer19
ENST00000374574.2:c.697del ENSP00000363702.2:p.Ser233ProfsTer19
ENST00000374580.8:c.697del ENSP00000363708.4:p.Ser233ProfsTer19
NM_001204.6:c.697del , LRG_712t1:c.697del NP_001195.2:p.Ser233ProfsTer19
XM_011511687.1:c.697del XP_011509989.1:p.Ser233ProfsTer19
XM_011511688.1:c.697del XP_011509990.1:p.Ser233ProfsTer19
NM_001204.7:c.697del MANE Select NP_001195.2:p.Ser233ProfsTer19