Canonical Allele Identifier: CA350344959
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202552858A>C , CM000664.2:g.202552858A>C GRCh38
NC_000002.11:g.203417581A>C , CM000664.1:g.203417581A>C GRCh37
NC_000002.10:g.203125826A>C NCBI36
NG_009363.1:g.181532A>C , LRG_712:g.181532A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1556A>C MANE Select ENSP00000363708.4:p.Asn519Thr
ENST00000638587.1:c.1487A>C ENSP00000491062.1:p.Asn496Thr
ENST00000374574.2:c.1556A>C ENSP00000363702.2:p.Asn519Thr
ENST00000374580.8:c.1556A>C ENSP00000363708.4:p.Asn519Thr
NM_001204.6:c.1556A>C , LRG_712t1:c.1556A>C NP_001195.2:p.Asn519Thr
XM_011511687.1:c.1556A>C XP_011509989.1:p.Asn519Thr
XM_011511688.1:c.1556A>C XP_011509990.1:p.Asn519Thr
NM_001204.7:c.1556A>C MANE Select NP_001195.2:p.Asn519Thr