Canonical Allele Identifier: CA16043210
Gene: CUL4B HGNC NCBI

Linked Data

ClinVar Variation Id: 372872
ClinVar RCV Id: RCV000414616
dbSNP Id: rs1057518039
MyVariant Identifiers: chrX:g.119694072T>C (hg19) chrX:g.120560217T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120560217T>C , CM000685.2:g.120560217T>C GRCh38
NC_000023.10:g.119694072T>C , CM000685.1:g.119694072T>C GRCh37
NC_000023.9:g.119578100T>C NCBI36
NG_009388.1:g.20613A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336592.11:c.437A>G ENSP00000338919.6:p.Asn146Ser
ENST00000371322.11:c.422A>G MANE Select ENSP00000360373.5:p.Asn141Ser
ENST00000404115.8:c.422A>G ENSP00000384109.4:p.Asn141Ser
ENST00000467641.2:n.89A>G
ENST00000673919.1:c.422A>G ENSP00000500994.1:p.Asn141Ser
ENST00000674137.11:c.422A>G ENSP00000501019.6:p.Asn141Ser
ENST00000679432.1:c.409A>G
ENST00000679927.1:c.77A>G ENSP00000505603.1:p.Asn26Ser
ENST00000680165.1:n.748A>G
ENST00000680324.1:n.336A>G
ENST00000680577.1:n.583A>G
ENST00000680673.1:c.476A>G ENSP00000505084.1:p.Asn159Ser
ENST00000681090.1:c.422A>G ENSP00000506288.1:p.Asn141Ser
ENST00000681206.1:c.437A>G ENSP00000505480.1:p.Asn146Ser
ENST00000681253.1:c.476A>G ENSP00000506259.1:p.Asn159Ser
ENST00000681333.1:c.422A>G ENSP00000505739.1:p.Asn141Ser
ENST00000681652.1:c.476A>G ENSP00000505176.1:p.Asn159Ser
ENST00000336592.10:c.437A>G ENSP00000338919.6:p.Asn146Ser
ENST00000371322.9:c.422A>G ENSP00000360373.5:p.Asn141Ser
ENST00000404115.7:c.476A>G ENSP00000384109.3:p.Asn159Ser
ENST00000467641.1:n.579A>G
NM_001079872.1:c.422A>G NP_001073341.1:p.Asn141Ser
NM_003588.3:c.476A>G NP_003579.3:p.Asn159Ser
XM_005262481.1:c.476A>G XP_005262538.1:p.Asn159Ser
XM_006724784.1:c.437A>G XP_006724847.1:p.Asn146Ser
XM_006724785.1:c.437A>G XP_006724848.1:p.Asn146Ser
NM_001330624.1:c.437A>G NP_001317553.1:p.Asn146Ser
NM_001079872.2:c.422A>G MANE Select NP_001073341.1:p.Asn141Ser
NM_001330624.2:c.437A>G NP_001317553.1:p.Asn146Ser
NM_003588.4:c.476A>G NP_003579.3:p.Asn159Ser
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