Canonical Allele Identifier: CA1839197750

Gene: CDKN2B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.22010170_22010171delinsTG , CM000671.2:g.22010170_22010171delinsTG	GRCh38
NC_000009.11:g.22010169_22010170delinsTG , CM000671.1:g.22010169_22010170delinsTG	GRCh37
NC_000009.10:g.22000169_22000170delinsTG	NCBI36
NG_023297.1:g.4143_4144delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-19263_348-19262delinsTG	ENSP00000385916.2:n.348-19263_348-19262delinsTG
ENST00000404796.2:c.348-19263_348-19262delinsTG	ENSP00000385916.2:n.348-19263_348-19262delinsTG
NR_003529.3:n.371+15009_371+15010delinsTG
NR_047532.1:n.371+15009_371+15010delinsTG
NR_047533.1:n.371+15009_371+15010delinsTG
NR_047534.1:n.371+15009_371+15010delinsTG
NR_047535.1:n.371+15009_371+15010delinsTG
NR_047536.1:n.371+15009_371+15010delinsTG
NR_047537.1:n.371+15009_371+15010delinsTG
NR_047538.1:n.371+15009_371+15010delinsTG
NR_047539.1:n.371+15009_371+15010delinsTG
NR_047540.1:n.371+15009_371+15010delinsTG
NR_047541.1:n.371+15009_371+15010delinsTG
NR_047542.1:n.371+15009_371+15010delinsTG
NR_047543.1:n.371+15009_371+15010delinsTG
NR_120536.1:n.371+15009_371+15010delinsTG