Canonical Allele Identifier: CA3848027
Gene: RHAG HGNC NCBI

Linked Data

dbSNP Id: rs781298167
ExAC: 6:49604558 C / T
gnomAD v2: 6-49604558-C-T
gnomAD v4: 6-49636845-C-T
MyVariant Identifiers: chr6:g.49604558C>T (hg19) chr6:g.49636845C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636845C>T , CM000668.2:g.49636845C>T GRCh38
NC_000006.11:g.49604558C>T , CM000668.1:g.49604558C>T GRCh37
NC_000006.10:g.49712517C>T NCBI36
NG_011704.1:g.5030G>A

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-33G>A NP_000315.2:n.-33G>A
XM_011514788.1:c.-33G>A XP_011513090.1:n.-33G>A
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