Canonical Allele Identifier: CA138804159
Gene: RHAG HGNC NCBI

Linked Data

dbSNP Id: rs1055252430
MyVariant Identifiers: chr6:g.49604553G>A (hg19) chr6:g.49636840G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636840G>A , CM000668.2:g.49636840G>A GRCh38
NC_000006.11:g.49604553G>A , CM000668.1:g.49604553G>A GRCh37
NC_000006.10:g.49712512G>A NCBI36
NG_011704.1:g.5035C>T

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-28C>T NP_000315.2:n.-28C>T
XM_011514788.1:c.-28C>T XP_011513090.1:n.-28C>T
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