Canonical Allele Identifier: CA2061483
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs371114044

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202555662A>G , CM000664.2:g.202555662A>G GRCh38
NC_000002.11:g.203420385A>G , CM000664.1:g.203420385A>G GRCh37
NC_000002.10:g.203128630A>G NCBI36
NG_009363.1:g.184336A>G , LRG_712:g.184336A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1997A>G MANE Select ENSP00000363708.4:p.Asn666Ser
ENST00000638587.1:c.1928A>G ENSP00000491062.1:n.1928A>G
ENST00000374574.2:c.1586+2774A>G ENSP00000363702.2:n.1586+2774A>G
ENST00000374580.8:c.1997A>G ENSP00000363708.4:p.Asn666Ser
NM_001204.6:c.1997A>G , LRG_712t1:c.1997A>G NP_001195.2:p.Asn666Ser
XM_011511687.1:c.1997A>G XP_011509989.1:p.Asn666Ser
XM_011511688.1:c.1586+2774A>G XP_011509990.1:n.1586+2774A>G
NM_001204.7:c.1997A>G MANE Select NP_001195.2:p.Asn666Ser