Canonical Allele Identifier: CA118946162

Gene: CDC20B

Linked Data

• dbSNP Id: rs373491856
• gnomAD v2: 5-54466465-T-G
• gnomAD v3: 5-55170637-T-G
• gnomAD v4: 5-55170637-T-G
• MyVariant Identifiers: chr5:g.54466465T>G (hg19) ; chr5:g.55170637T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55170637T>G , CM000667.2:g.55170637T>G	GRCh38
NC_000005.9:g.54466465T>G , CM000667.1:g.54466465T>G	GRCh37
NC_000005.8:g.54502222T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381375.7:c.126+1951A>C MANE Select	ENSP00000370781.2:n.126+1951A>C
ENST00000296733.5:c.126+1951A>C	ENSP00000296733.1:n.126+1951A>C
ENST00000322374.10:c.126+1951A>C	ENSP00000315720.6:n.126+1951A>C
ENST00000381375.6:c.126+1951A>C	ENSP00000370781.2:n.126+1951A>C
ENST00000507931.1:c.63+2301A>C	ENSP00000423919.1:n.63+2301A>C
ENST00000513180.5:c.126+1951A>C	ENSP00000426776.1:n.126+1951A>C
NM_001145734.2:c.126+1951A>C	NP_001139206.2:n.126+1951A>C
NM_001170402.1:c.126+1951A>C MANE Select	NP_001163873.1:n.126+1951A>C
NM_152623.2:c.126+1951A>C	NP_689836.2:n.126+1951A>C
XM_011543218.1:c.126+1951A>C	XP_011541520.1:n.126+1951A>C
XM_011543218.2:c.126+1951A>C	XP_011541520.1:n.126+1951A>C