Canonical Allele Identifier: CA2036281207
Gene: ACVR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51987174G= , CM000674.2:g.51987174G= GRCh38
NC_000012.11:g.52380958G= , CM000674.1:g.52380958G= GRCh37
NC_000012.10:g.50667225G= NCBI36
NG_022926.1:g.40508G=

Transcript Alleles

HGVS Amino-acid change
ENST00000257963.9:c.1261+232G= MANE Select ENSP00000257963.4:n.1261+232G=
ENST00000257963.8:c.1261+232G= ENSP00000257963.4:n.1261+232G=
ENST00000415850.6:c.1493G= ENSP00000397550.2:n.1493G=
ENST00000426655.6:c.1261+232G= ENSP00000390477.2:n.1261+232G=
ENST00000541224.5:c.1384+232G= ENSP00000442656.1:n.1384+232G=
ENST00000542485.1:c.1105+232G= ENSP00000442885.1:n.1105+232G=
ENST00000563121.1:n.289+1826G=
NM_004302.4:c.1261+232G= NP_004293.1:n.1261+232G=
NM_020327.3:c.1105+232G= NP_064732.3:n.1105+232G=
NM_020328.3:c.1384+232G= NP_064733.3:n.1384+232G=
XM_011538966.1:c.1259+1826G= XP_011537268.1:n.1259+1826G=
XM_011538966.3:c.1259+1826G= XP_011537268.1:n.1259+1826G=
XM_017020201.2:c.1136+1826G= XP_016875690.1:n.1136+1826G=
NM_004302.5:c.1261+232G= MANE Select NP_004293.1:n.1261+232G=
NM_020328.4:c.1384+232G= NP_064733.3:n.1384+232G=
NM_020327.4:c.1105+232G= NP_064732.3:n.1105+232G=