Canonical Allele Identifier: CA1215986709
Gene: RGS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811645A= , CM000663.2:g.192811645A= GRCh38
NC_000001.10:g.192780775A= , CM000663.1:g.192780775A= GRCh37
NC_000001.9:g.191047398A= NCBI36
NG_012800.1:g.7607A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*49A= MANE Select ENSP00000235382.5:n.*49A=
ENST00000235382.6:c.*49A= ENSP00000235382.5:n.*49A=
NM_002923.3:c.*49A= NP_002914.1:n.*49A=
NM_002923.4:c.*49A= MANE Select NP_002914.1:n.*49A=