Canonical Allele Identifier: CA1321560359
Gene: BMPR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556652A= , CM000664.2:g.202556652A= GRCh38
NC_000002.11:g.203421375A= , CM000664.1:g.203421375A= GRCh37
NC_000002.10:g.203129620A= NCBI36
NG_009363.1:g.185326A= , LRG_712:g.185326A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.2866+121A= MANE Select ENSP00000363708.4:n.2866+121A=
ENST00000638587.1:c.2797+121A= ENSP00000491062.1:n.2797+121A=
ENST00000374574.2:c.1587-3044A= ENSP00000363702.2:n.1587-3044A=
ENST00000374580.8:c.2866+121A= ENSP00000363708.4:n.2866+121A=
NM_001204.6:c.2866+121A= , LRG_712t1:c.2866+121A= NP_001195.2:n.2866+121A=
XM_011511687.1:c.2866+121A= XP_011509989.1:n.2866+121A=
XM_011511688.1:c.1587-3044A= XP_011509990.1:n.1587-3044A=
NM_001204.7:c.2866+121A= MANE Select NP_001195.2:n.2866+121A=