Canonical Allele Identifier: CA2649611375
Gene: RGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192811658_192811659del , CM000663.2:g.192811658_192811659del GRCh38
NC_000001.10:g.192780788_192780789del , CM000663.1:g.192780788_192780789del GRCh37
NC_000001.9:g.191047411_191047412del NCBI36
NG_012800.1:g.7620_7621del

Transcript Alleles

HGVS Amino-acid Change
ENST00000235382.7:c.*62_*63del MANE Select ENSP00000235382.5:n.*62_*63del
ENST00000235382.6:c.*62_*63del ENSP00000235382.5:n.*62_*63del
NM_002923.3:c.*62_*63del NP_002914.1:n.*62_*63del
NM_002923.4:c.*62_*63del MANE Select NP_002914.1:n.*62_*63del