Canonical Allele Identifier: CA645294005
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425736
ClinVar RCV Id: RCV000488624
dbSNP Id: rs368090069

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467516T>G , CM000664.2:g.202467516T>G GRCh38
NC_000002.11:g.203332239T>G , CM000664.1:g.203332239T>G GRCh37
NC_000002.10:g.203040484T>G NCBI36
NG_009363.1:g.96190T>G , LRG_712:g.96190T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.248-3T>G MANE Select ENSP00000363708.4:n.248-3T>G
ENST00000638587.1:c.179-3T>G ENSP00000491062.1:n.179-3T>G
ENST00000374574.2:c.248-3T>G ENSP00000363702.2:n.248-3T>G
ENST00000374580.8:c.248-3T>G ENSP00000363708.4:n.248-3T>G
ENST00000479069.1:n.155-3T>G
NM_001204.6:c.248-3T>G , LRG_712t1:c.248-3T>G NP_001195.2:n.248-3T>G
XM_011511687.1:c.248-3T>G XP_011509989.1:n.248-3T>G
XM_011511688.1:c.248-3T>G XP_011509990.1:n.248-3T>G
NM_001204.7:c.248-3T>G MANE Select NP_001195.2:n.248-3T>G