Canonical Allele Identifier: CA15074535
Gene: OTUD7B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12048493

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149955122A>C , CM000663.2:g.149955122A>C GRCh38
NC_000001.10:g.149927034A>C , CM000663.1:g.149927034A>C GRCh37
NC_000001.9:g.148193658A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_020205.3:c.845+4562T>G VV NP_064590.2:p.=
XM_011509782.1:c.845+4562T>G XP_011508084.1:p.=
XM_011509783.1:c.845+4562T>G XP_011508085.1:p.=
XM_011509784.1:c.845+4562T>G XP_011508086.1:p.=
XM_011509785.1:c.845+4562T>G XP_011508087.1:p.=
XM_011509786.1:c.608+4562T>G XP_011508088.1:p.=
XM_011509787.1:c.608+4562T>G XP_011508089.1:p.=
XM_011509788.1:c.608+4562T>G XP_011508090.1:p.=
XM_011509784.3:c.845+4562T>G
XM_011509785.2:c.845+4562T>G
XM_011509788.2:c.608+4562T>G
XM_017001850.1:c.608+4562T>G XP_016857339.1:p.=
XM_017001851.2:c.458+4562T>G XP_016857340.1:p.=
XM_024448516.1:c.458+4562T>G XP_024304284.1:p.=
ENST00000417191.2:c.845+4562T>G ENSP00000408231.1:p.=
ENST00000581312.5:c.845+4562T>G ENSP00000462729.1:p.=