Canonical Allele Identifier: CA1321474685
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202377509C= , CM000664.2:g.202377509C= GRCh38
NC_000002.11:g.203242232C= , CM000664.1:g.203242232C= GRCh37
NC_000002.10:g.202950477C= NCBI36
NG_009363.1:g.6183C= , LRG_712:g.6183C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.35C= MANE Select ENSP00000363708.4:p.Pro12=
ENST00000374574.2:c.35C= ENSP00000363702.2:p.Pro12=
ENST00000374580.8:c.35C= ENSP00000363708.4:p.Pro12=
NM_001204.6:c.35C= , LRG_712t1:c.35C= NP_001195.2:p.Pro12=
XM_011511687.1:c.35C= XP_011509989.1:p.Pro12=
XM_011511688.1:c.35C= XP_011509990.1:p.Pro12=
NM_001204.7:c.35C= MANE Select NP_001195.2:p.Pro12=