Canonical Allele Identifier: CA350399552
Gene: BMPR2 HGNC NCBI

Linked Data

COSMIC: COSM265521
MyVariant Identifiers: chr2:g.203332262G>C (hg19) chr2:g.202467539G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467539G>C , CM000664.2:g.202467539G>C GRCh38
NC_000002.11:g.203332262G>C , CM000664.1:g.203332262G>C GRCh37
NC_000002.10:g.203040507G>C NCBI36
NG_009363.1:g.96213G>C , LRG_712:g.96213G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.268G>C MANE Select ENSP00000363708.4:p.Asp90His
ENST00000638587.1:c.199G>C ENSP00000491062.1:p.Asp67His
ENST00000374574.2:c.268G>C ENSP00000363702.2:p.Asp90His
ENST00000374580.8:c.268G>C ENSP00000363708.4:p.Asp90His
ENST00000479069.1:n.175G>C
NM_001204.6:c.268G>C , LRG_712t1:c.268G>C NP_001195.2:p.Asp90His
XM_011511687.1:c.268G>C XP_011509989.1:p.Asp90His
XM_011511688.1:c.268G>C XP_011509990.1:p.Asp90His
NM_001204.7:c.268G>C MANE Select NP_001195.2:p.Asp90His
Search 100 bp 5'
Search 100 bp 3'