Canonical Allele Identifier: CA2578642964
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636841A>G , CM000668.2:g.49636841A>G GRCh38
NC_000006.11:g.49604554A>G , CM000668.1:g.49604554A>G GRCh37
NC_000006.10:g.49712513A>G NCBI36
NG_011704.1:g.5034T>C

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-29T>C NP_000315.2:n.-29T>C
XM_011514788.1:c.-29T>C XP_011513090.1:n.-29T>C