Canonical Allele Identifier: CA669463665

Gene: BMPR1A

Linked Data

• dbSNP Id: rs1244877468
• gnomAD v3: 10-86875941-T-C
• gnomAD v4: 10-86875941-T-C
• MyVariant Identifiers: chr10:g.88635698T>C (hg19) ; chr10:g.86875941T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86875941T>C , CM000672.2:g.86875941T>C	GRCh38
NC_000010.10:g.88635698T>C , CM000672.1:g.88635698T>C	GRCh37
NC_000010.9:g.88625678T>C	NCBI36
NG_009362.1:g.124303T>C , LRG_298:g.124303T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480152.3:c.-78T>C	ENSP00000483569.2:n.-78T>C
ENST00000635816.2:c.-78T>C	ENSP00000489707.1:n.-78T>C
ENST00000636056.2:c.-78T>C	ENSP00000490273.1:n.-78T>C
ENST00000372037.8:c.-78T>C MANE Select	ENSP00000361107.2:n.-78T>C
ENST00000635816.1:c.-78T>C	ENSP00000489707.1:n.-78T>C
ENST00000636056.1:c.-78T>C	ENSP00000490273.1:n.-78T>C
ENST00000638429.1:c.-78T>C	ENSP00000492290.1:n.-78T>C
ENST00000372037.7:c.-78T>C	ENSP00000361107.1:n.-78T>C
ENST00000480152.2:c.-78T>C	ENSP00000483569.1:n.-78T>C
NM_004329.2:c.-78T>C , LRG_298t1:c.-78T>C	NP_004320.2:n.-78T>C
XM_011540103.1:c.-78T>C	XP_011538405.1:n.-78T>C
XM_011540104.1:c.-78T>C	XP_011538406.1:n.-78T>C
XM_011540103.2:c.-78T>C	XP_011538405.1:n.-78T>C
XM_011540104.2:c.-78T>C	XP_011538406.1:n.-78T>C
NM_004329.3:c.-78T>C MANE Select	NP_004320.2:n.-78T>C