Canonical Allele Identifier: CA586899222

Gene: CDKN2B-AS1

Linked Data

• dbSNP Id: rs1388901412
• gnomAD v2: 9-22000443-T-C
• gnomAD v3: 9-22000444-T-C
• gnomAD v4: 9-22000444-T-C
• MyVariant Identifiers: chr9:g.22000443T>C (hg19) ; chr9:g.22000444T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22000444T>C , CM000671.2:g.22000444T>C	GRCh38
NC_000009.11:g.22000443T>C , CM000671.1:g.22000443T>C	GRCh37
NC_000009.10:g.21990443T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-28989T>C	ENSP00000385916.2:n.348-28989T>C
ENST00000404796.2:c.348-28989T>C	ENSP00000385916.2:n.348-28989T>C
NR_003529.3:n.371+5283T>C
NR_047532.1:n.371+5283T>C
NR_047533.1:n.371+5283T>C
NR_047534.1:n.371+5283T>C
NR_047535.1:n.371+5283T>C
NR_047536.1:n.371+5283T>C
NR_047537.1:n.371+5283T>C
NR_047538.1:n.371+5283T>C
NR_047539.1:n.371+5283T>C
NR_047540.1:n.371+5283T>C
NR_047541.1:n.371+5283T>C
NR_047542.1:n.371+5283T>C
NR_047543.1:n.371+5283T>C
NR_120536.1:n.371+5283T>C