Canonical Allele Identifier: CA684979874

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs1300505886
• gnomAD v3: 12-12717686-T-C
• gnomAD v4: 12-12717686-T-C
• MyVariant Identifiers: chr12:g.12870620T>C (hg19) ; chr12:g.12717686T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717686T>C , CM000674.2:g.12717686T>C	GRCh38
NC_000012.11:g.12870620T>C , CM000674.1:g.12870620T>C	GRCh37
NC_000012.10:g.12761887T>C	NCBI36
NG_016341.1:g.5319T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-154T>C (CDKN1B)	ENSP00000507272.1:n.-154T>C
ENST00000682620.1:n.1631-1139T>C (CDKN1B)
ENST00000684771.1:n.585-1139T>C (CDKN1B)
ENST00000228872.9:c.-154T>C (CDKN1B) MANE Select	ENSP00000228872.4:n.-154T>C
ENST00000228872.8:c.-154T>C (CDKN1B)	ENSP00000228872.4:n.-154T>C
ENST00000477087.1:n.155-1139T>C (CDKN1B)
NM_004064.4:c.-154T>C (CDKN1B)	NP_004055.1:n.-154T>C
XM_011520623.3:c.-2180A>G (GPR19)	XP_011518925.1:n.-2180A>G
XM_017019216.2:c.-2208A>G (GPR19)	XP_016874705.1:n.-2208A>G
NM_004064.5:c.-154T>C (CDKN1B) MANE Select	NP_004055.1:n.-154T>C