Canonical Allele Identifier: CA2038154770

Gene: RAB5B SUOX

Linked Data

• dbSNP Id: rs34962186

Genomic Alleles

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

Transcript Alleles

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