Canonical Allele Identifier: CA509687801
Gene: BMP2 HGNC NCBI

Linked Data

dbSNP Id: rs1360955611
gnomAD v3: 20-6770138-G-C
gnomAD v4: 20-6770138-G-C
MyVariant Identifiers: chr20:g.6750785G>C (hg19) chr20:g.6770138G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6770138G>C , CM000682.2:g.6770138G>C GRCh38
NC_000020.10:g.6750785G>C , CM000682.1:g.6750785G>C GRCh37
NC_000020.9:g.6698785G>C NCBI36
NG_023233.1:g.7041G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378827.5:c.12G>C MANE Select ENSP00000368104.3:p.Gly4=
ENST00000378827.4:c.12G>C ENSP00000368104.3:p.Gly4=
NM_001200.2:c.12G>C NP_001191.1:p.Gly4=
XM_011529323.1:c.-123+1263G>C XP_011527625.1:n.-123+1263G>C
NM_001200.3:c.12G>C NP_001191.1:p.Gly4=
NM_001200.4:c.12G>C MANE Select NP_001191.1:p.Gly4=
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Search 100 bp 3'