Canonical Allele Identifier: CA2618861796

Gene: ACVR1B

Linked Data

• gnomAD v4: 12-51987256-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51987256C>A , CM000674.2:g.51987256C>A	GRCh38
NC_000012.11:g.52381040C>A , CM000674.1:g.52381040C>A	GRCh37
NC_000012.10:g.50667307C>A	NCBI36
NG_022926.1:g.40590C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257963.9:c.1261+314C>A MANE Select	ENSP00000257963.4:n.1261+314C>A
ENST00000257963.8:c.1261+314C>A	ENSP00000257963.4:n.1261+314C>A
ENST00000415850.6:c.1575C>A	ENSP00000397550.2:n.1575C>A
ENST00000426655.6:c.1261+314C>A	ENSP00000390477.2:n.1261+314C>A
ENST00000541224.5:c.1384+314C>A	ENSP00000442656.1:n.1384+314C>A
ENST00000542485.1:c.1105+314C>A	ENSP00000442885.1:n.1105+314C>A
ENST00000563121.1:n.289+1908C>A
NM_004302.4:c.1261+314C>A	NP_004293.1:n.1261+314C>A
NM_020327.3:c.1105+314C>A	NP_064732.3:n.1105+314C>A
NM_020328.3:c.1384+314C>A	NP_064733.3:n.1384+314C>A
XM_011538966.1:c.1259+1908C>A	XP_011537268.1:n.1259+1908C>A
XM_011538966.3:c.1259+1908C>A	XP_011537268.1:n.1259+1908C>A
XM_017020201.2:c.1136+1908C>A	XP_016875690.1:n.1136+1908C>A
NM_004302.5:c.1261+314C>A MANE Select	NP_004293.1:n.1261+314C>A
NM_020328.4:c.1384+314C>A	NP_064733.3:n.1384+314C>A
NM_020327.4:c.1105+314C>A	NP_064732.3:n.1105+314C>A