Canonical Allele Identifier: CA350399830
Gene: BMPR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.203332385T>C (hg19) chr2:g.202467662T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467662T>C , CM000664.2:g.202467662T>C GRCh38
NC_000002.11:g.203332385T>C , CM000664.1:g.203332385T>C GRCh37
NC_000002.10:g.203040630T>C NCBI36
NG_009363.1:g.96336T>C , LRG_712:g.96336T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374580.10:c.391T>C MANE Select ENSP00000363708.4:p.Phe131Leu
ENST00000638587.1:c.322T>C ENSP00000491062.1:p.Phe108Leu
ENST00000374574.2:c.391T>C ENSP00000363702.2:p.Phe131Leu
ENST00000374580.8:c.391T>C ENSP00000363708.4:p.Phe131Leu
ENST00000479069.1:n.298T>C
NM_001204.6:c.391T>C , LRG_712t1:c.391T>C NP_001195.2:p.Phe131Leu
XM_011511687.1:c.391T>C XP_011509989.1:p.Phe131Leu
XM_011511688.1:c.391T>C XP_011509990.1:p.Phe131Leu
NM_001204.7:c.391T>C MANE Select NP_001195.2:p.Phe131Leu
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