Canonical Allele Identifier: CA350399681
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1692351533

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467600A>G , CM000664.2:g.202467600A>G GRCh38
NC_000002.11:g.203332323A>G , CM000664.1:g.203332323A>G GRCh37
NC_000002.10:g.203040568A>G NCBI36
NG_009363.1:g.96274A>G , LRG_712:g.96274A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.329A>G MANE Select ENSP00000363708.4:p.Asn110Ser
ENST00000638587.1:c.260A>G ENSP00000491062.1:p.Asn87Ser
ENST00000374574.2:c.329A>G ENSP00000363702.2:p.Asn110Ser
ENST00000374580.8:c.329A>G ENSP00000363708.4:p.Asn110Ser
ENST00000479069.1:n.236A>G
NM_001204.6:c.329A>G , LRG_712t1:c.329A>G NP_001195.2:p.Asn110Ser
XM_011511687.1:c.329A>G XP_011509989.1:p.Asn110Ser
XM_011511688.1:c.329A>G XP_011509990.1:p.Asn110Ser
NM_001204.7:c.329A>G MANE Select NP_001195.2:p.Asn110Ser