Canonical Allele Identifier: CA915941496
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812942
ClinVar RCV Id: RCV001003878

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202465783_202470694del , CM000664.2:g.202465783_202470694del GRCh38
NC_000002.11:g.203330506_203335417del , CM000664.1:g.203330506_203335417del GRCh37
NC_000002.10:g.203038751_203043662del NCBI36
NG_009363.1:g.94457_99368del , LRG_712:g.94457_99368del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.247+804_418+3005del
ENST00000638587.1:c.176+800_349+3005del
ENST00000374574.2:c.247+804_418+3005del
ENST00000374580.8:c.247+804_418+3005del
ENST00000479069.1:n.154+804_325+3005del
NM_001204.6:c.247+804_418+3005del , LRG_712t1:c.247+804_418+3005del
XM_011511687.1:c.247+804_418+3005del
XM_011511688.1:c.247+804_418+3005del
NM_001204.7:c.247+804_418+3005del