Canonical Allele Identifier: CA509818019
Gene: BMP2 HGNC NCBI

Linked Data

gnomAD v4: 20-6778534-T-G
MyVariant Identifiers: chr20:g.6759181T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6778534T>G , CM000682.2:g.6778534T>G GRCh38
NC_000020.10:g.6759181T>G , CM000682.1:g.6759181T>G GRCh37
NC_000020.9:g.6707181T>G NCBI36
NG_023233.1:g.15437T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378827.5:c.636T>G MANE Select ENSP00000368104.3:p.Ala212=
ENST00000378827.4:c.636T>G ENSP00000368104.3:p.Ala212=
NM_001200.2:c.636T>G NP_001191.1:p.Ala212=
XM_011529323.1:c.168T>G XP_011527625.1:p.Ala56=
NM_001200.3:c.636T>G NP_001191.1:p.Ala212=
NM_001200.4:c.636T>G MANE Select NP_001191.1:p.Ala212=