Canonical Allele Identifier: CA350399055
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202464835G>C , CM000664.2:g.202464835G>C GRCh38
NC_000002.11:g.203329558G>C , CM000664.1:g.203329558G>C GRCh37
NC_000002.10:g.203037803G>C NCBI36
NG_009363.1:g.93509G>C , LRG_712:g.93509G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.103G>C MANE Select ENSP00000363708.4:p.Ala35Pro
ENST00000638587.1:c.28G>C ENSP00000491062.1:p.Ala10Pro
ENST00000374574.2:c.103G>C ENSP00000363702.2:p.Ala35Pro
ENST00000374580.8:c.103G>C ENSP00000363708.4:p.Ala35Pro
ENST00000479069.1:n.10G>C
NM_001204.6:c.103G>C , LRG_712t1:c.103G>C NP_001195.2:p.Ala35Pro
XM_011511687.1:c.103G>C XP_011509989.1:p.Ala35Pro
XM_011511688.1:c.103G>C XP_011509990.1:p.Ala35Pro
NM_001204.7:c.103G>C MANE Select NP_001195.2:p.Ala35Pro