Canonical Allele Identifier: CA684979963
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

dbSNP Id: rs1388947450
gnomAD v4: 12-12717773-CTTTGT-C
MyVariant Identifiers: chr12:g.12870708_12870712del (hg19) chr12:g.12717774_12717778del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717780_12717784del , CM000674.2:g.12717780_12717784del GRCh38
NC_000012.11:g.12870714_12870718del , CM000674.1:g.12870714_12870718del GRCh37
NC_000012.10:g.12761981_12761985del NCBI36
NG_016341.1:g.5413_5417del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-60_-56del (CDKN1B) ENSP00000507272.1:n.-60_-56del
ENST00000682620.1:n.1631-1045_1631-1041del (CDKN1B)
ENST00000684771.1:n.585-1045_585-1041del (CDKN1B)
ENST00000228872.9:c.-60_-56del (CDKN1B) MANE Select ENSP00000228872.4:n.-60_-56del
ENST00000228872.8:c.-60_-56del (CDKN1B) ENSP00000228872.4:n.-60_-56del
ENST00000477087.1:n.155-1045_155-1041del (CDKN1B)
NM_004064.4:c.-60_-56del (CDKN1B) NP_004055.1:n.-60_-56del
XM_011520623.3:c.-2272_-2268del (GPR19) XP_011518925.1:n.-2272_-2268del
XM_017019216.2:c.-2300_-2296del (GPR19) XP_016874705.1:n.-2300_-2296del
NM_004064.5:c.-60_-56del (CDKN1B) MANE Select NP_004055.1:n.-60_-56del
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