Canonical Allele Identifier: CA1321474551
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1690170030

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202377301_202377319del , CM000664.2:g.202377301_202377319del GRCh38
NC_000002.11:g.203242024_203242042del , CM000664.1:g.203242024_203242042del GRCh37
NC_000002.10:g.202950269_202950287del NCBI36
NG_009363.1:g.5975_5993del , LRG_712:g.5975_5993del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.-174_-156del MANE Select ENSP00000363708.4:n.-174_-156del
ENST00000374580.8:c.-174_-156del ENSP00000363708.4:n.-174_-156del
NM_001204.6:c.-174_-156del , LRG_712t1:c.-174_-156del NP_001195.2:n.-174_-156del
XM_011511687.1:c.-174_-156del XP_011509989.1:n.-174_-156del
XM_011511688.1:c.-174_-156del XP_011509990.1:n.-174_-156del
NM_001204.7:c.-174_-156del MANE Select NP_001195.2:n.-174_-156del