Canonical Allele Identifier: CA2038155076

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55995509T= , CM000674.2:g.55995509T= GRCh38
NC_000012.11:g.56389293T= , CM000674.1:g.56389293T= GRCh37
NC_000012.10:g.54675560T= NCBI36
NG_008136.1:g.3251T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360299.10:c.*3297T= (RAB5B) MANE Select ENSP00000353444.5:n.*3297T=
ENST00000360299.9:c.*3297T= (RAB5B) ENSP00000353444.5:n.*3297T=
NM_001252036.1:c.*3297T= (RAB5B) NP_001238965.1:n.*3297T=
NM_001252037.1:c.*3297T= (RAB5B) NP_001238966.1:n.*3297T=
NM_002868.3:c.*3297T= (RAB5B) NP_002859.1:n.*3297T=
XM_017019905.2:c.-2118T= (SUOX) XP_016875394.1:n.-2118T=
XM_017019907.2:c.-2208T= (SUOX) XP_016875396.1:n.-2208T=
XM_024449167.1:c.-1992T= (SUOX) XP_024304935.1:n.-1992T=
NM_002868.4:c.*3297T= (RAB5B) MANE Select NP_002859.1:n.*3297T=
NM_001252036.2:c.*3297T= (RAB5B) NP_001238965.1:n.*3297T=
NM_001252037.2:c.*3297T= (RAB5B) NP_001238966.1:n.*3297T=