Canonical Allele Identifier: CA526022780

Gene: OTUD7B

Linked Data

• dbSNP Id: rs1553774266
• gnomAD v2: 1-149926915-T-G
• gnomAD v3: 1-149955003-T-G
• gnomAD v4: 1-149955003-T-G
• MyVariant Identifiers: chr1:g.149926915T>G (hg19) ; chr1:g.149955003T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149955003T>G , CM000663.2:g.149955003T>G	GRCh38
NC_000001.10:g.149926915T>G , CM000663.1:g.149926915T>G	GRCh37
NC_000001.9:g.148193539T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000581312.6:c.845+4681A>C MANE Select	ENSP00000462729.1:n.845+4681A>C
ENST00000417191.2:c.845+4681A>C	ENSP00000408231.1:n.845+4681A>C
ENST00000581312.5:c.845+4681A>C	ENSP00000462729.1:n.845+4681A>C
NM_020205.3:c.845+4681A>C	NP_064590.2:n.845+4681A>C
XM_011509782.1:c.845+4681A>C	XP_011508084.1:n.845+4681A>C
XM_011509783.1:c.845+4681A>C	XP_011508085.1:n.845+4681A>C
XM_011509784.1:c.845+4681A>C	XP_011508086.1:n.845+4681A>C
XM_011509785.1:c.845+4681A>C	XP_011508087.1:n.845+4681A>C
XM_011509786.1:c.608+4681A>C	XP_011508088.1:n.608+4681A>C
XM_011509787.1:c.608+4681A>C	XP_011508089.1:n.608+4681A>C
XM_011509788.1:c.608+4681A>C	XP_011508090.1:n.608+4681A>C
XM_011509784.3:c.845+4681A>C	XP_011508086.1:n.845+4681A>C
XM_011509785.2:c.845+4681A>C	XP_011508087.1:n.845+4681A>C
XM_011509788.2:c.608+4681A>C	XP_011508090.1:n.608+4681A>C
XM_017001850.1:c.608+4681A>C	XP_016857339.1:n.608+4681A>C
XM_017001851.2:c.458+4681A>C	XP_016857340.1:n.458+4681A>C
XM_024448516.1:c.458+4681A>C	XP_024304284.1:n.458+4681A>C
NM_020205.4:c.845+4681A>C MANE Select	NP_064590.2:n.845+4681A>C