Canonical Allele Identifier: CA339821187

Gene: BMP8B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.39788305G>C , CM000663.2:g.39788305G>C	GRCh38
NC_000001.10:g.40253977G>C , CM000663.1:g.40253977G>C	GRCh37
NC_000001.9:g.40026564G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001720.5:c.181C>G MANE Select	NP_001711.2:p.Arg61Gly
ENST00000372827.8:c.181C>G MANE Select	ENSP00000361915.3:p.Arg61Gly
NM_001720.3:c.181C>G	NP_001711.2:p.Arg61Gly
NM_001720.4:c.181C>G	NP_001711.2:p.Arg61Gly
ENST00000372827.7:c.181C>G	ENSP00000361915.3:p.Arg61Gly
ENST00000397360.2:c.181C>G	ENSP00000380518.2:p.Arg61Gly
XM_005271149.3:c.181C>G	XP_005271206.1:p.Arg61Gly
XM_005271149.4:c.181C>G	XP_005271206.1:p.Arg61Gly
XM_011542022.1:c.181C>G	XP_011540324.1:p.Arg61Gly
XM_011542022.2:c.181C>G	XP_011540324.1:p.Arg61Gly
XM_011542024.1:c.181C>G	XP_011540326.1:p.Arg61Gly
XM_011542024.2:c.181C>G	XP_011540326.2:p.Arg61Gly
XM_011542025.1:c.181C>G	XP_011540327.1:p.Arg61Gly
XM_011542025.2:c.181C>G	XP_011540327.1:p.Arg61Gly
XM_011542545.1:c.897+68G>C	XP_011540847.1:n.897+68G>C
XM_017002155.1:c.181C>G	XP_016857644.1:p.Arg61Gly
XM_017002156.1:c.181C>G	XP_016857645.1:p.Arg61Gly
XR_946748.1:n.186C>G
XR_946748.2:n.275C>G
XR_946749.1:n.186C>G
XR_946749.2:n.275C>G
XR_946750.1:n.186C>G
XR_946750.2:n.275C>G