Canonical Allele Identifier: CA916754262

Gene: BMPR2

Linked Data

• dbSNP Id: rs1559046511
• gnomAD v4: 2-202464793-ATTTCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202464797_202464801del , CM000664.2:g.202464797_202464801del	GRCh38
NC_000002.11:g.203329520_203329524del , CM000664.1:g.203329520_203329524del	GRCh37
NC_000002.10:g.203037765_203037769del	NCBI36
NG_009363.1:g.93471_93475del , LRG_712:g.93471_93475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374580.10:c.77-12_77-8del MANE Select	ENSP00000363708.4:n.77-12_77-8del
ENST00000374574.2:c.77-12_77-8del	ENSP00000363702.2:n.77-12_77-8del
ENST00000374580.8:c.77-12_77-8del	ENSP00000363708.4:n.77-12_77-8del
NM_001204.6:c.77-12_77-8del , LRG_712t1:c.77-12_77-8del	NP_001195.2:n.77-12_77-8del
XM_011511687.1:c.77-12_77-8del	XP_011509989.1:n.77-12_77-8del
XM_011511688.1:c.77-12_77-8del	XP_011509990.1:n.77-12_77-8del
NM_001204.7:c.77-12_77-8del MANE Select	NP_001195.2:n.77-12_77-8del