Canonical Allele Identifier: CA190747691

Gene: CDKN2B-AS1

Linked Data

• dbSNP Id: rs186647683
• gnomAD v2: 9-21997921-A-G
• gnomAD v3: 9-21997922-A-G
• gnomAD v4: 9-21997922-A-G
• MyVariant Identifiers: chr9:g.21997921A>G (hg19) ; chr9:g.21997922A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21997922A>G , CM000671.2:g.21997922A>G	GRCh38
NC_000009.11:g.21997921A>G , CM000671.1:g.21997921A>G	GRCh37
NC_000009.10:g.21987921A>G	NCBI36
NG_007485.1:g.1570T>C , LRG_11:g.1570T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000404796.3:c.348-31511A>G	ENSP00000385916.2:n.348-31511A>G
ENST00000404796.2:c.348-31511A>G	ENSP00000385916.2:n.348-31511A>G
NR_003529.3:n.371+2761A>G
NR_047532.1:n.371+2761A>G
NR_047533.1:n.371+2761A>G
NR_047534.1:n.371+2761A>G
NR_047535.1:n.371+2761A>G
NR_047536.1:n.371+2761A>G
NR_047537.1:n.371+2761A>G
NR_047538.1:n.371+2761A>G
NR_047539.1:n.371+2761A>G
NR_047540.1:n.371+2761A>G
NR_047541.1:n.371+2761A>G
NR_047542.1:n.371+2761A>G
NR_047543.1:n.371+2761A>G
NR_120536.1:n.371+2761A>G