Canonical Allele Identifier: CA862189548
Gene: CDKN2B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1479299386

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21997873_21997874insA , CM000671.2:g.21997873_21997874insA GRCh38
NC_000009.11:g.21997872_21997873insA , CM000671.1:g.21997872_21997873insA GRCh37
NC_000009.10:g.21987872_21987873insA NCBI36
NG_007485.1:g.1618_1619insT , LRG_11:g.1618_1619insT

Transcript Alleles

HGVS Amino-acid change
ENST00000404796.3:c.348-31560_348-31559insA ENSP00000385916.2:n.348-31560_348-31559insA
ENST00000404796.2:c.348-31560_348-31559insA ENSP00000385916.2:n.348-31560_348-31559insA
NR_003529.3:n.371+2712_371+2713insA
NR_047532.1:n.371+2712_371+2713insA
NR_047533.1:n.371+2712_371+2713insA
NR_047534.1:n.371+2712_371+2713insA
NR_047535.1:n.371+2712_371+2713insA
NR_047536.1:n.371+2712_371+2713insA
NR_047537.1:n.371+2712_371+2713insA
NR_047538.1:n.371+2712_371+2713insA
NR_047539.1:n.371+2712_371+2713insA
NR_047540.1:n.371+2712_371+2713insA
NR_047541.1:n.371+2712_371+2713insA
NR_047542.1:n.371+2712_371+2713insA
NR_047543.1:n.371+2712_371+2713insA
NR_120536.1:n.371+2712_371+2713insA