Canonical Allele Identifier: CA2679055069
Gene: RHAG HGNC NCBI

Linked Data

gnomAD v4: 6-49636846-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636846T>C , CM000668.2:g.49636846T>C GRCh38
NC_000006.11:g.49604559T>C , CM000668.1:g.49604559T>C GRCh37
NC_000006.10:g.49712518T>C NCBI36
NG_011704.1:g.5029A>G

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-34A>G NP_000315.2:n.-34A>G
XM_011514788.1:c.-34A>G XP_011513090.1:n.-34A>G
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