Canonical Allele Identifier: CA684979921

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs1489255128
• MyVariant Identifiers: chr12:g.12870682G>C (hg19) ; chr12:g.12717748G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717748G>C , CM000674.2:g.12717748G>C	GRCh38
NC_000012.11:g.12870682G>C , CM000674.1:g.12870682G>C	GRCh37
NC_000012.10:g.12761949G>C	NCBI36
NG_016341.1:g.5381G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.-92G>C (CDKN1B)	ENSP00000507272.1:n.-92G>C
ENST00000682620.1:n.1631-1077G>C (CDKN1B)
ENST00000684771.1:n.585-1077G>C (CDKN1B)
ENST00000228872.9:c.-92G>C (CDKN1B) MANE Select	ENSP00000228872.4:n.-92G>C
ENST00000228872.8:c.-92G>C (CDKN1B)	ENSP00000228872.4:n.-92G>C
ENST00000477087.1:n.155-1077G>C (CDKN1B)
NM_004064.4:c.-92G>C (CDKN1B)	NP_004055.1:n.-92G>C
XM_011520623.3:c.-2242C>G (GPR19)	XP_011518925.1:n.-2242C>G
XM_017019216.2:c.-2270C>G (GPR19)	XP_016874705.1:n.-2270C>G
NM_004064.5:c.-92G>C (CDKN1B) MANE Select	NP_004055.1:n.-92G>C