Canonical Allele Identifier: CA567156161

Gene: RHAG

Linked Data

• dbSNP Id: rs1327138914
• gnomAD v2: 6-49586753-CCATT-C
• gnomAD v3: 6-49619040-CCATT-C
• gnomAD v4: 6-49619040-CCATT-C
• MyVariant Identifiers: chr6:g.49586754_49586757del (hg19) ; chr6:g.49619041_49619044del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49619044_49619047del , CM000668.2:g.49619044_49619047del	GRCh38
NC_000006.11:g.49586757_49586760del , CM000668.1:g.49586757_49586760del	GRCh37
NC_000006.10:g.49694716_49694719del	NCBI36
NG_011704.1:g.22831_22834del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+135_341+138del MANE Select	ENSP00000360217.4:n.341+135_341+138del
ENST00000642530.1:n.616+135_616+138del
ENST00000646272.1:c.341+135_341+138del	ENSP00000494337.1:n.341+135_341+138del
ENST00000646939.1:c.341+135_341+138del	ENSP00000494709.1:n.341+135_341+138del
ENST00000646963.1:c.341+135_341+138del	ENSP00000495337.1:n.341+135_341+138del
ENST00000229810.9:c.341+135_341+138del	ENSP00000229810.8:n.341+135_341+138del
ENST00000371175.8:c.341+135_341+138del	ENSP00000360217.4:n.341+135_341+138del
ENST00000618248.3:c.341+135_341+138del	ENSP00000482984.1:n.341+135_341+138del
NM_000324.2:c.341+135_341+138del	NP_000315.2:n.341+135_341+138del
XM_011514788.1:c.341+135_341+138del	XP_011513090.1:n.341+135_341+138del
NM_000324.3:c.341+135_341+138del MANE Select	NP_000315.2:n.341+135_341+138del