Canonical Allele Identifier: CA350399531

Gene: BMPR2

Linked Data

• MyVariant Identifiers: chr2:g.203332253C>T (hg19) ; chr2:g.202467530C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.202467530C>T , CM000664.2:g.202467530C>T	GRCh38
NC_000002.11:g.203332253C>T , CM000664.1:g.203332253C>T	GRCh37
NC_000002.10:g.203040498C>T	NCBI36
NG_009363.1:g.96204C>T , LRG_712:g.96204C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374580.10:c.259C>T MANE Select	ENSP00000363708.4:p.His87Tyr
ENST00000638587.1:c.190C>T	ENSP00000491062.1:p.His64Tyr
ENST00000374574.2:c.259C>T	ENSP00000363702.2:p.His87Tyr
ENST00000374580.8:c.259C>T	ENSP00000363708.4:p.His87Tyr
ENST00000479069.1:n.166C>T
NM_001204.6:c.259C>T , LRG_712t1:c.259C>T	NP_001195.2:p.His87Tyr
XM_011511687.1:c.259C>T	XP_011509989.1:p.His87Tyr
XM_011511688.1:c.259C>T	XP_011509990.1:p.His87Tyr
NM_001204.7:c.259C>T MANE Select	NP_001195.2:p.His87Tyr