Canonical Allele Identifier: CA1839187237
Gene: CDKN2B-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.22000241_22000244delinsCTTG , CM000671.2:g.22000241_22000244delinsCTTG GRCh38
NC_000009.11:g.22000240_22000243delinsCTTG , CM000671.1:g.22000240_22000243delinsCTTG GRCh37
NC_000009.10:g.21990240_21990243delinsCTTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.348-29192_348-29189delinsCTTG ENSP00000385916.2:n.348-29192_348-29189delinsCTTG
ENST00000404796.2:c.348-29192_348-29189delinsCTTG ENSP00000385916.2:n.348-29192_348-29189delinsCTTG
NR_003529.3:n.371+5080_371+5083delinsCTTG
NR_047532.1:n.371+5080_371+5083delinsCTTG
NR_047533.1:n.371+5080_371+5083delinsCTTG
NR_047534.1:n.371+5080_371+5083delinsCTTG
NR_047535.1:n.371+5080_371+5083delinsCTTG
NR_047536.1:n.371+5080_371+5083delinsCTTG
NR_047537.1:n.371+5080_371+5083delinsCTTG
NR_047538.1:n.371+5080_371+5083delinsCTTG
NR_047539.1:n.371+5080_371+5083delinsCTTG
NR_047540.1:n.371+5080_371+5083delinsCTTG
NR_047541.1:n.371+5080_371+5083delinsCTTG
NR_047542.1:n.371+5080_371+5083delinsCTTG
NR_047543.1:n.371+5080_371+5083delinsCTTG
NR_120536.1:n.371+5080_371+5083delinsCTTG