Canonical Allele Identifier: CA889181290

Gene: OTUD7B

Linked Data

• dbSNP Id: rs1344581293
• gnomAD v3: 1-149954983-T-C
• gnomAD v4: 1-149954983-T-C
• MyVariant Identifiers: chr1:g.149954983T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149954983T>C , CM000663.2:g.149954983T>C	GRCh38
NC_000001.10:g.149926895T>C , CM000663.1:g.149926895T>C	GRCh37
NC_000001.9:g.148193519T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000581312.6:c.845+4701A>G MANE Select	ENSP00000462729.1:n.845+4701A>G
ENST00000417191.2:c.845+4701A>G	ENSP00000408231.1:n.845+4701A>G
ENST00000581312.5:c.845+4701A>G	ENSP00000462729.1:n.845+4701A>G
NM_020205.3:c.845+4701A>G	NP_064590.2:n.845+4701A>G
XM_011509782.1:c.845+4701A>G	XP_011508084.1:n.845+4701A>G
XM_011509783.1:c.845+4701A>G	XP_011508085.1:n.845+4701A>G
XM_011509784.1:c.845+4701A>G	XP_011508086.1:n.845+4701A>G
XM_011509785.1:c.845+4701A>G	XP_011508087.1:n.845+4701A>G
XM_011509786.1:c.608+4701A>G	XP_011508088.1:n.608+4701A>G
XM_011509787.1:c.608+4701A>G	XP_011508089.1:n.608+4701A>G
XM_011509788.1:c.608+4701A>G	XP_011508090.1:n.608+4701A>G
XM_011509784.3:c.845+4701A>G	XP_011508086.1:n.845+4701A>G
XM_011509785.2:c.845+4701A>G	XP_011508087.1:n.845+4701A>G
XM_011509788.2:c.608+4701A>G	XP_011508090.1:n.608+4701A>G
XM_017001850.1:c.608+4701A>G	XP_016857339.1:n.608+4701A>G
XM_017001851.2:c.458+4701A>G	XP_016857340.1:n.458+4701A>G
XM_024448516.1:c.458+4701A>G	XP_024304284.1:n.458+4701A>G
NM_020205.4:c.845+4701A>G MANE Select	NP_064590.2:n.845+4701A>G