Canonical Allele Identifier: CA364397505
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 438647
ClinVar RCV Id: RCV000505587
dbSNP Id: rs1554172605
MyVariant Identifiers: chr6:g.49578797A>G (hg19) chr6:g.49611084A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49611084A>G , CM000668.2:g.49611084A>G GRCh38
NC_000006.11:g.49578797A>G , CM000668.1:g.49578797A>G GRCh37
NC_000006.10:g.49686756A>G NCBI36
NG_011704.1:g.30791T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.1007T>C MANE Select ENSP00000360217.4:p.Leu336Ser
ENST00000646272.1:c.1007T>C ENSP00000494337.1:p.Leu336Ser
ENST00000646939.1:c.945+1313T>C ENSP00000494709.1:n.945+1313T>C
ENST00000646963.1:c.1007T>C ENSP00000495337.1:p.Leu336Ser
ENST00000229810.9:c.1007T>C ENSP00000229810.8:p.Leu336Ser
ENST00000371175.8:c.1007T>C ENSP00000360217.4:p.Leu336Ser
ENST00000618248.3:c.1007T>C ENSP00000482984.1:p.Leu336Ser
NM_000324.2:c.1007T>C NP_000315.2:p.Leu336Ser
NM_000324.3:c.1007T>C MANE Select NP_000315.2:p.Leu336Ser
Search 100 bp 5'
Search 100 bp 3'