Canonical Allele Identifier: CA1321510326
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1692346932

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467458_202467460del , CM000664.2:g.202467458_202467460del GRCh38
NC_000002.11:g.203332181_203332183del , CM000664.1:g.203332181_203332183del GRCh37
NC_000002.10:g.203040426_203040428del NCBI36
NG_009363.1:g.96132_96134del , LRG_712:g.96132_96134del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.248-61_248-59del MANE Select ENSP00000363708.4:n.248-61_248-59del
ENST00000638587.1:c.179-61_179-59del ENSP00000491062.1:n.179-61_179-59del
ENST00000374574.2:c.248-61_248-59del ENSP00000363702.2:n.248-61_248-59del
ENST00000374580.8:c.248-61_248-59del ENSP00000363708.4:n.248-61_248-59del
ENST00000479069.1:n.155-61_155-59del
NM_001204.6:c.248-61_248-59del , LRG_712t1:c.248-61_248-59del NP_001195.2:n.248-61_248-59del
XM_011511687.1:c.248-61_248-59del XP_011509989.1:n.248-61_248-59del
XM_011511688.1:c.248-61_248-59del XP_011509990.1:n.248-61_248-59del
NM_001204.7:c.248-61_248-59del MANE Select NP_001195.2:n.248-61_248-59del