Canonical Allele Identifier: CA2017031824

Gene: GPR19

Linked Data

• dbSNP Id: rs10845606

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12681960C>G , CM000674.2:g.12681960C>G	GRCh38
NC_000012.11:g.12834894C>G , CM000674.1:g.12834894C>G	GRCh37
NC_000012.10:g.12726161C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651487.1:c.-23+2391G>C MANE Select	ENSP00000498976.1:n.-23+2391G>C
ENST00000332427.6:c.-23+2391G>C	ENSP00000333744.2:n.-23+2391G>C
ENST00000540510.1:c.-23+2391G>C	ENSP00000441832.1:n.-23+2391G>C
ENST00000540796.5:c.-23+2391G>C	ENSP00000441963.1:n.-23+2391G>C
NM_006143.2:c.-23+2391G>C	NP_006134.1:n.-23+2391G>C
XM_011520622.1:c.6+2391G>C	XP_011518924.1:n.6+2391G>C
XM_011520623.1:c.6+2391G>C	XP_011518925.1:n.6+2391G>C
XM_011520624.1:c.6+2391G>C	XP_011518926.1:n.6+2391G>C
XM_011520625.1:c.-162+2391G>C	XP_011518927.1:n.-162+2391G>C
XM_011520626.1:c.562+2391G>C	XP_011518928.1:n.562+2391G>C
XM_011520623.3:c.6+2391G>C	XP_011518925.1:n.6+2391G>C
XM_011520624.2:c.6+2391G>C	XP_011518926.1:n.6+2391G>C
XM_011520625.2:c.-162+2391G>C	XP_011518927.1:n.-162+2391G>C
XM_017019212.1:c.6+2391G>C	XP_016874701.1:n.6+2391G>C
XM_017019213.1:c.6+2391G>C	XP_016874702.1:n.6+2391G>C
XM_017019214.1:c.6+2391G>C	XP_016874703.1:n.6+2391G>C
XM_017019216.2:c.-23+2391G>C	XP_016874705.1:n.-23+2391G>C
NM_006143.3:c.-23+2391G>C MANE Select	NP_006134.2:n.-23+2391G>C