Canonical Allele Identifier: CA1215986762
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811798C= , CM000663.2:g.192811798C= GRCh38
NC_000001.10:g.192780928C= , CM000663.1:g.192780928C= GRCh37
NC_000001.9:g.191047551C= NCBI36
NG_012800.1:g.7760C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*202C= MANE Select ENSP00000235382.5:n.*202C=
ENST00000235382.6:c.*202C= ENSP00000235382.5:n.*202C=
NM_002923.3:c.*202C= NP_002914.1:n.*202C=
NM_002923.4:c.*202C= MANE Select NP_002914.1:n.*202C=