Canonical Allele Identifier: CA2061284
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs553523967

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202530898C>G , CM000664.2:g.202530898C>G GRCh38
NC_000002.11:g.203395621C>G , CM000664.1:g.203395621C>G GRCh37
NC_000002.10:g.203103866C>G NCBI36
NG_009363.1:g.159572C>G , LRG_712:g.159572C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.1072C>G MANE Select ENSP00000363708.4:p.Leu358Val
ENST00000638587.1:c.1003C>G ENSP00000491062.1:p.Leu335Val
ENST00000374574.2:c.1072C>G ENSP00000363702.2:p.Leu358Val
ENST00000374580.8:c.1072C>G ENSP00000363708.4:p.Leu358Val
NM_001204.6:c.1072C>G , LRG_712t1:c.1072C>G NP_001195.2:p.Leu358Val
XM_011511687.1:c.1072C>G XP_011509989.1:p.Leu358Val
XM_011511688.1:c.1072C>G XP_011509990.1:p.Leu358Val
NM_001204.7:c.1072C>G MANE Select NP_001195.2:p.Leu358Val