Canonical Allele Identifier: CA509817891
Gene: BMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1049007
MyVariant Identifiers: chr20:g.6751034A>C (hg19) chr20:g.6770387A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6770387A>C , CM000682.2:g.6770387A>C GRCh38
NC_000020.10:g.6751034A>C , CM000682.1:g.6751034A>C GRCh37
NC_000020.9:g.6699034A>C NCBI36
NG_023233.1:g.7290A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378827.5:c.261A>C MANE Select ENSP00000368104.3:p.Ser87=
ENST00000378827.4:c.261A>C ENSP00000368104.3:p.Ser87=
NM_001200.2:c.261A>C NP_001191.1:p.Ser87=
XM_011529323.1:c.-123+1512A>C XP_011527625.1:n.-123+1512A>C
NM_001200.3:c.261A>C NP_001191.1:p.Ser87=
NM_001200.4:c.261A>C MANE Select NP_001191.1:p.Ser87=
Search 100 bp 5'
Search 100 bp 3'