Canonical Allele Identifier: CA944839812
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

dbSNP Id: rs1473000886
gnomAD v3: 12-12717566-A-ACCCTCTCCGCTTGCCTGGTC
gnomAD v4: 12-12717566-A-ACCCTCTCCGCTTGCCTGGTC
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717575_12717594dup , CM000674.2:g.12717575_12717594dup GRCh38
NC_000012.11:g.12870509_12870528dup , CM000674.1:g.12870509_12870528dup GRCh37
NC_000012.10:g.12761776_12761795dup NCBI36
NG_016341.1:g.5208_5227dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-265_-246dup (CDKN1B) ENSP00000507272.1:n.-265_-246dup
ENST00000682620.1:n.1631-1250_1631-1231dup (CDKN1B)
ENST00000684771.1:n.585-1250_585-1231dup (CDKN1B)
ENST00000228872.9:c.-265_-246dup (CDKN1B) MANE Select ENSP00000228872.4:n.-265_-246dup
ENST00000228872.8:c.-265_-246dup (CDKN1B) ENSP00000228872.4:n.-265_-246dup
ENST00000477087.1:n.155-1250_155-1231dup (CDKN1B)
NM_004064.4:c.-265_-246dup (CDKN1B) NP_004055.1:n.-265_-246dup
XM_011520623.3:c.-2080_-2061dup (GPR19) XP_011518925.1:n.-2080_-2061dup
XM_017019216.2:c.-2108_-2089dup (GPR19) XP_016874705.1:n.-2108_-2089dup
NM_004064.5:c.-265_-246dup (CDKN1B) MANE Select NP_004055.1:n.-265_-246dup
Search 100 bp 5'
Search 100 bp 3'