Canonical Allele Identifier: CA350341341
Gene: BMPR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530827T>C , CM000664.2:g.202530827T>C GRCh38
NC_000002.11:g.203395550T>C , CM000664.1:g.203395550T>C GRCh37
NC_000002.10:g.203103795T>C NCBI36
NG_009363.1:g.159501T>C , LRG_712:g.159501T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.1001T>C MANE Select ENSP00000363708.4:p.Leu334Ser
ENST00000638587.1:c.932T>C ENSP00000491062.1:p.Leu311Ser
ENST00000374574.2:c.1001T>C ENSP00000363702.2:p.Leu334Ser
ENST00000374580.8:c.1001T>C ENSP00000363708.4:p.Leu334Ser
NM_001204.6:c.1001T>C , LRG_712t1:c.1001T>C NP_001195.2:p.Leu334Ser
XM_011511687.1:c.1001T>C XP_011509989.1:p.Leu334Ser
XM_011511688.1:c.1001T>C XP_011509990.1:p.Leu334Ser
NM_001204.7:c.1001T>C MANE Select NP_001195.2:p.Leu334Ser