Canonical Allele Identifier: CA2747137547

Gene: RGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192812194_192812195insGT , CM000663.2:g.192812194_192812195insGT	GRCh38
NC_000001.10:g.192781324_192781325insGT , CM000663.1:g.192781324_192781325insGT	GRCh37
NC_000001.9:g.191047947_191047948insGT	NCBI36
NG_012800.1:g.8156_8157insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235382.7:c.*598_*599insGT MANE Select	ENSP00000235382.5:n.*598_*599insGT
ENST00000235382.6:c.*598_*599insGT	ENSP00000235382.5:n.*598_*599insGT
NM_002923.3:c.*598_*599insGT	NP_002914.1:n.*598_*599insGT
NM_002923.4:c.*598_*599insGT MANE Select	NP_002914.1:n.*598_*599insGT