Canonical Allele Identifier: CA350349368
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203421077G>A (hg19) chr2:g.202556354G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202556354G>A , CM000664.2:g.202556354G>A GRCh38
NC_000002.11:g.203421077G>A , CM000664.1:g.203421077G>A GRCh37
NC_000002.10:g.203129322G>A NCBI36
NG_009363.1:g.185028G>A , LRG_712:g.185028G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.2689G>A MANE Select ENSP00000363708.4:p.Gly897Ser
ENST00000638587.1:c.2620G>A ENSP00000491062.1:n.2620G>A
ENST00000374574.2:c.1587-3342G>A ENSP00000363702.2:n.1587-3342G>A
ENST00000374580.8:c.2689G>A ENSP00000363708.4:p.Gly897Ser
NM_001204.6:c.2689G>A , LRG_712t1:c.2689G>A NP_001195.2:p.Gly897Ser
XM_011511687.1:c.2689G>A XP_011509989.1:p.Gly897Ser
XM_011511688.1:c.1587-3342G>A XP_011509990.1:n.1587-3342G>A
NM_001204.7:c.2689G>A MANE Select NP_001195.2:p.Gly897Ser
Search 100 bp 5'
Search 100 bp 3'