ClinGen Allele Registry
Allele Registry
Pathogenicity Calculator
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Canonical Allele Identifier:
CA254358
Gene: BMPR1A
HGNC
NCBI
Identifiers and link-outs to other resources
ClinVar Variation Id:
8231
ClinVar RCV Id:
RCV000008714
dbSNP Id:
rs199476085
MyVariant Identifiers:
chr10:g.88677027G>A (hg19)
chr10:g.86917270G>A (hg38)
User contributed link-outs
Pubmed:
PMID:11381269
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Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.86917270G>A , CM000672.2:g.86917270G>A
GRCh38
NC_000010.10:g.88677027G>A , CM000672.1:g.88677027G>A
GRCh37
NC_000010.9:g.88667007G>A
NCBI36
NG_009362.1:g.165632G>A , LRG_298:g.165632G>A
Transcript Alleles
HGVS
Amino-acid change
NM_004329.2:c.812G>A , LRG_298t1:c.812G>A
NP_004320.2:p.Trp271Ter
XM_011540103.1:c.812G>A
XP_011538405.1:p.Trp271Ter
XM_011540104.1:c.812G>A
XP_011538406.1:p.Trp271Ter
XM_011540103.2:c.812G>A
XM_011540104.2:c.812G>A
ENST00000372037.7:c.812G>A
ENSP00000361107.1:p.Trp271Ter
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