Canonical Allele Identifier: CA377455119

Gene: BMPR1A

Linked Data

• ClinVar Variation Id: 2603362
• ClinVar RCV Id: RCV003354569
• MyVariant Identifiers: chr10:g.88672122G>T (hg19) ; chr10:g.86912365G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86912365G>T , CM000672.2:g.86912365G>T	GRCh38
NC_000010.10:g.88672122G>T , CM000672.1:g.88672122G>T	GRCh37
NC_000010.9:g.88662102G>T	NCBI36
NG_009362.1:g.160727G>T , LRG_298:g.160727G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.656G>T	ENSP00000483569.2:p.Gly219Val
ENST00000635816.2:c.656G>T	ENSP00000489707.1:p.Gly219Val
ENST00000636056.2:c.656G>T	ENSP00000490273.1:p.Gly219Val
ENST00000372037.8:c.656G>T MANE Select	ENSP00000361107.2:p.Gly219Val
ENST00000635816.1:c.656G>T	ENSP00000489707.1:p.Gly219Val
ENST00000636056.1:c.656G>T	ENSP00000490273.1:p.Gly219Val
ENST00000638429.1:c.656G>T	ENSP00000492290.1:p.Gly219Val
ENST00000372037.7:c.656G>T	ENSP00000361107.1:p.Gly219Val
NM_004329.2:c.656G>T , LRG_298t1:c.656G>T	NP_004320.2:p.Gly219Val
XM_011540103.1:c.656G>T	XP_011538405.1:p.Gly219Val
XM_011540104.1:c.656G>T	XP_011538406.1:p.Gly219Val
XM_011540103.2:c.656G>T	XP_011538405.1:p.Gly219Val
XM_011540104.2:c.656G>T	XP_011538406.1:p.Gly219Val
NM_004329.3:c.656G>T MANE Select	NP_004320.2:p.Gly219Val