Canonical Allele Identifier: CA10581912
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238628
dbSNP Id: rs878854272

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530951_202530970del , CM000664.2:g.202530951_202530970del GRCh38
NC_000002.11:g.203395674_203395693del , CM000664.1:g.203395674_203395693del GRCh37
NC_000002.10:g.203103919_203103938del NCBI36
NG_009363.1:g.159625_159644del , LRG_712:g.159625_159644del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1125_1128+16del
ENST00000638587.1:c.1056_1059+16del
ENST00000374574.2:c.1125_1128+16del
ENST00000374580.8:c.1125_1128+16del
NM_001204.6:c.1125_1128+16del , LRG_712t1:c.1125_1128+16del
XM_011511687.1:c.1125_1128+16del
XM_011511688.1:c.1125_1128+16del
NM_001204.7:c.1125_1128+16del