Canonical Allele Identifier: CA64016383
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs377096548
MyVariant Identifiers: chr2:g.203384514T>G (hg19) chr2:g.202519791T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202519791T>G , CM000664.2:g.202519791T>G GRCh38
NC_000002.11:g.203384514T>G , CM000664.1:g.203384514T>G GRCh37
NC_000002.10:g.203092759T>G NCBI36
NG_009363.1:g.148465T>G , LRG_712:g.148465T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.853-296T>G MANE Select ENSP00000363708.4:n.853-296T>G
ENST00000638587.1:c.784-296T>G ENSP00000491062.1:n.784-296T>G
ENST00000374574.2:c.853-296T>G ENSP00000363702.2:n.853-296T>G
ENST00000374580.8:c.853-296T>G ENSP00000363708.4:n.853-296T>G
NM_001204.6:c.853-296T>G , LRG_712t1:c.853-296T>G NP_001195.2:n.853-296T>G
XM_011511687.1:c.853-296T>G XP_011509989.1:n.853-296T>G
XM_011511688.1:c.853-296T>G XP_011509990.1:n.853-296T>G
NM_001204.7:c.853-296T>G MANE Select NP_001195.2:n.853-296T>G
Search 100 bp 5'
Search 100 bp 3'