Canonical Allele Identifier: CA350340732
Gene: BMPR2 HGNC NCBI

Linked Data

dbSNP Id: rs1334341372

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202520111C>T , CM000664.2:g.202520111C>T GRCh38
NC_000002.11:g.203384834C>T , CM000664.1:g.203384834C>T GRCh37
NC_000002.10:g.203093079C>T NCBI36
NG_009363.1:g.148785C>T , LRG_712:g.148785C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.877C>T MANE Select ENSP00000363708.4:p.Leu293Phe
ENST00000638587.1:c.808C>T ENSP00000491062.1:p.Leu270Phe
ENST00000374574.2:c.877C>T ENSP00000363702.2:p.Leu293Phe
ENST00000374580.8:c.877C>T ENSP00000363708.4:p.Leu293Phe
NM_001204.6:c.877C>T , LRG_712t1:c.877C>T NP_001195.2:p.Leu293Phe
XM_011511687.1:c.877C>T XP_011509989.1:p.Leu293Phe
XM_011511688.1:c.877C>T XP_011509990.1:p.Leu293Phe
NM_001204.7:c.877C>T MANE Select NP_001195.2:p.Leu293Phe