Canonical Allele Identifier: CA12604866
Gene: HDAC9 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12666612

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.18335622T>C , CM000669.2:g.18335622T>C GRCh38
NC_000007.13:g.18375245T>C , CM000669.1:g.18375245T>C GRCh37
NC_000007.12:g.18341770T>C NCBI36
NG_023250.2:g.253674T>C
NG_023250.3:g.253674T>C

Transcript Alleles

HGVS Amino-acid change
NM_001204144.1:c.26-123220T>C VV NP_001191073.1:p.=
XM_011515626.1:c.100+45107T>C XP_011513928.1:p.=
XM_011515627.1:c.16+45107T>C XP_011513929.1:p.=
XM_011515628.1:c.16+45107T>C XP_011513930.1:p.=
XM_011515629.1:c.16+45107T>C XP_011513931.1:p.=
XM_011515630.1:c.16+45107T>C XP_011513932.1:p.=
XM_011515631.1:c.26-160640T>C XP_011513933.1:p.=
XM_011515632.1:c.16+45107T>C XP_011513934.1:p.=
XM_011515633.1:c.16+45107T>C XP_011513935.1:p.=
XM_011515634.1:c.16+45107T>C XP_011513936.1:p.=
XM_011515647.1:c.16+45107T>C XP_011513949.1:p.=
XM_011515650.1:c.16+45107T>C XP_011513952.1:p.=
XM_011515651.1:c.16+45107T>C XP_011513953.1:p.=
XR_926952.1:n.75+45107T>C
NM_001204144.2:c.26-123220T>C VV NP_001191073.1:p.=
NM_001321868.1:c.26-160640T>C VV NP_001308797.1:p.=
NM_001321869.1:c.26-160640T>C VV NP_001308798.1:p.=
NM_001321870.1:c.26-160640T>C VV NP_001308799.1:p.=
NM_001321871.1:c.26-160640T>C VV NP_001308800.1:p.=
NM_001321872.1:c.26-160640T>C VV NP_001308801.1:p.=
NM_001321873.1:c.26-160640T>C VV NP_001308802.1:p.=
NM_001321896.1:c.-194+45107T>C VV NP_001308825.1:p.=
ENST00000413509.6:c.-42+45107T>C ENSP00000412497.2:p.=
ENST00000417496.6:c.26-123220T>C ENSP00000401669.2:p.=
ENST00000433709.6:c.-111+45107T>C ENSP00000409003.2:p.=
ENST00000461159.6:n.94+45107T>C
ENST00000474742.1:n.66+45107T>C