Canonical Allele Identifier: CA1215986748
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811747A= , CM000663.2:g.192811747A= GRCh38
NC_000001.10:g.192780877A= , CM000663.1:g.192780877A= GRCh37
NC_000001.9:g.191047500A= NCBI36
NG_012800.1:g.7709A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*151A= MANE Select ENSP00000235382.5:n.*151A=
ENST00000235382.6:c.*151A= ENSP00000235382.5:n.*151A=
NM_002923.3:c.*151A= NP_002914.1:n.*151A=
NM_002923.4:c.*151A= MANE Select NP_002914.1:n.*151A=