Canonical Allele Identifier: CA944839942
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

dbSNP Id: rs1565419148

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717695G>T , CM000674.2:g.12717695G>T GRCh38
NC_000012.11:g.12870629G>T , CM000674.1:g.12870629G>T GRCh37
NC_000012.10:g.12761896G>T NCBI36
NG_016341.1:g.5328G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-145G>T (CDKN1B) ENSP00000507272.1:n.-145G>T
ENST00000682620.1:n.1631-1130G>T (CDKN1B)
ENST00000684771.1:n.585-1130G>T (CDKN1B)
ENST00000228872.9:c.-145G>T (CDKN1B) MANE Select ENSP00000228872.4:n.-145G>T
ENST00000228872.8:c.-145G>T (CDKN1B) ENSP00000228872.4:n.-145G>T
ENST00000477087.1:n.155-1130G>T (CDKN1B)
NM_004064.4:c.-145G>T (CDKN1B) NP_004055.1:n.-145G>T
XM_011520623.3:c.-2189C>A (GPR19) XP_011518925.1:n.-2189C>A
XM_017019216.2:c.-2217C>A (GPR19) XP_016874705.1:n.-2217C>A
NM_004064.5:c.-145G>T (CDKN1B) MANE Select NP_004055.1:n.-145G>T