Canonical Allele Identifier: CA2679055076
Gene: RHAG HGNC NCBI

Linked Data

gnomAD v4: 6-49636873-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636873A>G , CM000668.2:g.49636873A>G GRCh38
NC_000006.11:g.49604586A>G , CM000668.1:g.49604586A>G GRCh37
NC_000006.10:g.49712545A>G NCBI36
NG_011704.1:g.5002T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000324.2:c.-61T>C NP_000315.2:n.-61T>C
XM_011514788.1:c.-61T>C XP_011513090.1:n.-61T>C
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