Canonical Allele Identifier: CA16619003
Gene: BMPR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 422893
ClinVar RCV Id: RCV003762749
dbSNP Id: rs1064796072

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86917134del , CM000672.2:g.86917134del GRCh38
NC_000010.10:g.88676891del , CM000672.1:g.88676891del GRCh37
NC_000010.9:g.88666871del NCBI36
NG_009362.1:g.165496del , LRG_298:g.165496del

Transcript Alleles

HGVS Amino-acid change
ENST00000480152.3:c.676del
ENST00000635816.2:c.676del
ENST00000636056.2:c.676del
ENST00000372037.8:c.676del
ENST00000635816.1:c.676del
ENST00000636056.1:c.676del
ENST00000638429.1:c.676del
ENST00000372037.7:c.676del
NM_004329.2:c.676del , LRG_298t1:c.676del
XM_011540103.1:c.676del
XM_011540104.1:c.676del
XM_011540103.2:c.676del
XM_011540104.2:c.676del
NM_004329.3:c.676del