Canonical Allele Identifier: CA11991008
Gene: RGS14 HGNC NCBI
MyVariant.info:
GRCh38 chr5:g.177367190G>A
GRCh37 chr5:g.176794191G>A
gnomAD v2:
5:176794191 G / A
gnomAD v3:
5:177367190 G / A
gnomAD v4:
chr5-177367190-G-A
Joint Max Group AF 0.42154842 (SAS)
Genomes Max Group AF 0.40073823 (SAS)
Exomes Max Group AF 0.4221717 (SAS)
dbSNP:
12654812
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177367190G>A , CM000667.2:g.177367190G>A GRCh38
NC_000005.9:g.176794191G>A , CM000667.1:g.176794191G>A GRCh37
NC_000005.8:g.176726797G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000408923.8:c.483+156G>A MANE Select ENSP00000386229.3:n.483+156G>A
ENST00000408923.7:c.483+156G>A ENSP00000386229.3:n.483+156G>A
ENST00000504631.5:n.517+156G>A
ENST00000511890.1:c.92+156G>A
ENST00000514713.5:n.92+156G>A
NM_006480.4:c.483+156G>A NP_006471.2:n.483+156G>A
XM_005265794.3:c.483+156G>A XP_005265851.1:n.483+156G>A
XM_005265795.3:c.483+156G>A XP_005265852.1:n.483+156G>A
NM_001366617.1:c.483+156G>A NP_001353546.1:n.483+156G>A
NM_001366618.1:c.483+156G>A NP_001353547.1:n.483+156G>A
XM_024454328.1:c.483+156G>A XP_024310096.1:n.483+156G>A
NM_006480.5:c.483+156G>A MANE Select NP_006471.2:n.483+156G>A
Search 100 bp 5'
Search 100 bp 3'