Canonical Allele Identifier: CA2038154769
Community Standard Title: NM_002868.4(RAB5B):c.*2893T=

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55995105T= , CM000674.2:g.55995105T= GRCh38
NC_000012.11:g.56388889T= , CM000674.1:g.56388889T= GRCh37
NC_000012.10:g.54675156T= NCBI36
NG_008136.1:g.2847T=

Transcript Alleles

HGVS Amino-acid Change
NM_002868.4:c.*2893T= (RAB5B) MANE Select NP_002859.1:n.*2893T=
ENST00000360299.10:c.*2893T= (RAB5B) MANE Select ENSP00000353444.5:n.*2893T=
NM_001252036.1:c.*2893T= (RAB5B) NP_001238965.1:n.*2893T=
NM_001252036.2:c.*2893T= (RAB5B) NP_001238965.1:n.*2893T=
NM_001252037.1:c.*2893T= (RAB5B) NP_001238966.1:n.*2893T=
NM_001252037.2:c.*2893T= (RAB5B) NP_001238966.1:n.*2893T=
NM_002868.3:c.*2893T= (RAB5B) NP_002859.1:n.*2893T=
ENST00000360299.9:c.*2893T= (RAB5B) ENSP00000353444.5:n.*2893T=
XM_017019905.2:c.-2522T= (SUOX) XP_016875394.1:n.-2522T=
XM_017019907.2:c.-2612T= (SUOX) XP_016875396.1:n.-2612T=
XM_024449167.1:c.-2396T= (SUOX) XP_024304935.1:n.-2396T=