Canonical Allele Identifier: CA2207312882
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10877046G= , CM000678.2:g.10877046G= GRCh38
NC_000016.9:g.10970903G= , CM000678.1:g.10970903G= GRCh37
NC_000016.8:g.10878404G= NCBI36
NG_009628.1:g.4849G= , LRG_49:g.4849G=

Transcript Alleles

HGVS Amino-acid change
ENST00000636238.1:c.-21+10727G= ENSP00000490205.1:n.-21+10727G=
ENST00000637439.1:c.283+10474G= ENSP00000489907.1:n.283+10474G=
XM_006720880.2:c.346+10474G= XP_006720943.2:n.346+10474G=
XM_011522484.1:c.346+10474G= XP_011520786.1:n.346+10474G=
XM_011522485.1:c.346+10474G= XP_011520787.1:n.346+10474G=
XM_011522486.1:c.346+10474G= XP_011520788.1:n.346+10474G=
XM_011522487.1:c.247+10474G= XP_011520789.1:n.247+10474G=
XM_011522489.1:c.247+10474G= XP_011520791.1:n.247+10474G=
XM_011522491.1:c.346+10474G= XP_011520793.1:n.346+10474G=
XM_011522494.1:c.-21+10727G= XP_011520796.1:n.-21+10727G=
XR_932841.1:n.361+10474G=
XR_932842.1:n.361+10474G=
XR_932843.1:n.361+10474G=
XR_932846.1:n.361+10474G=
XR_932847.1:n.361+10474G=
XR_933067.1:n.1162+11269C=
XR_933068.1:n.1162+11269C=
XM_006720880.3:c.346+10474G= XP_006720943.2:n.346+10474G=
XM_011522484.3:c.346+10474G= XP_011520786.1:n.346+10474G=
XM_011522485.2:c.346+10474G= XP_011520787.1:n.346+10474G=
XM_011522486.2:c.346+10474G= XP_011520788.1:n.346+10474G=
XM_011522487.2:c.247+10474G= XP_011520789.1:n.247+10474G=
XM_011522489.2:c.247+10474G= XP_011520791.1:n.247+10474G=
XM_011522491.2:c.346+10474G= XP_011520793.1:n.346+10474G=
XM_011522494.2:c.-21+10727G= XP_011520796.1:n.-21+10727G=
XR_001751904.1:n.365+10474G=
XR_002957860.1:n.1246+11269C=
XR_002957861.1:n.1246+11269C=
XR_002957863.1:n.1442+5973C=
XR_932841.3:n.363+10474G=
XR_932842.2:n.363+10474G=
XR_932846.3:n.365+10474G=
XR_932847.3:n.365+10474G=