Canonical Allele Identifier: CA350399695

Gene: BMPR2

Linked Data

• MyVariant Identifiers: chr2:g.203332329C>G (hg19) ; chr2:g.202467606C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202467606C>G , CM000664.2:g.202467606C>G	GRCh38
NC_000002.11:g.203332329C>G , CM000664.1:g.203332329C>G	GRCh37
NC_000002.10:g.203040574C>G	NCBI36
NG_009363.1:g.96280C>G , LRG_712:g.96280C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374580.10:c.335C>G MANE Select	ENSP00000363708.4:p.Thr112Arg
ENST00000638587.1:c.266C>G	ENSP00000491062.1:p.Thr89Arg
ENST00000374574.2:c.335C>G	ENSP00000363702.2:p.Thr112Arg
ENST00000374580.8:c.335C>G	ENSP00000363708.4:p.Thr112Arg
ENST00000479069.1:n.242C>G
NM_001204.6:c.335C>G , LRG_712t1:c.335C>G	NP_001195.2:p.Thr112Arg
XM_011511687.1:c.335C>G	XP_011509989.1:p.Thr112Arg
XM_011511688.1:c.335C>G	XP_011509990.1:p.Thr112Arg
NM_001204.7:c.335C>G MANE Select	NP_001195.2:p.Thr112Arg