Canonical Allele Identifier: CA350399072
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464839T>A , CM000664.2:g.202464839T>A GRCh38
NC_000002.11:g.203329562T>A , CM000664.1:g.203329562T>A GRCh37
NC_000002.10:g.203037807T>A NCBI36
NG_009363.1:g.93513T>A , LRG_712:g.93513T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.107T>A MANE Select ENSP00000363708.4:p.Phe36Tyr
ENST00000638587.1:c.32T>A ENSP00000491062.1:p.Phe11Tyr
ENST00000374574.2:c.107T>A ENSP00000363702.2:p.Phe36Tyr
ENST00000374580.8:c.107T>A ENSP00000363708.4:p.Phe36Tyr
ENST00000479069.1:n.14T>A
NM_001204.6:c.107T>A , LRG_712t1:c.107T>A NP_001195.2:p.Phe36Tyr
XM_011511687.1:c.107T>A XP_011509989.1:p.Phe36Tyr
XM_011511688.1:c.107T>A XP_011509990.1:p.Phe36Tyr
NM_001204.7:c.107T>A MANE Select NP_001195.2:p.Phe36Tyr