Canonical Allele Identifier: CA3848026

Gene: RHAG

Linked Data

• dbSNP Id: rs754859329
• ExAC: 6:49604546 G / A
• gnomAD v2: 6-49604546-G-A
• gnomAD v3: 6-49636833-G-A
• gnomAD v4: 6-49636833-G-A
• MyVariant Identifiers: chr6:g.49604546G>A (hg19) ; chr6:g.49636833G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49636833G>A , CM000668.2:g.49636833G>A	GRCh38
NC_000006.11:g.49604546G>A , CM000668.1:g.49604546G>A	GRCh37
NC_000006.10:g.49712505G>A	NCBI36
NG_011704.1:g.5042C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.-21C>T MANE Select	ENSP00000360217.4:n.-21C>T
ENST00000642530.1:n.7C>T
ENST00000646272.1:c.-21C>T	ENSP00000494337.1:n.-21C>T
ENST00000646939.1:c.-21C>T	ENSP00000494709.1:n.-21C>T
ENST00000646963.1:c.-21C>T	ENSP00000495337.1:n.-21C>T
ENST00000229810.9:c.-21C>T	ENSP00000229810.8:n.-21C>T
ENST00000371175.8:c.-21C>T	ENSP00000360217.4:n.-21C>T
ENST00000618248.3:c.-21C>T	ENSP00000482984.1:n.-21C>T
NM_000324.2:c.-21C>T	NP_000315.2:n.-21C>T
XM_011514788.1:c.-21C>T	XP_011513090.1:n.-21C>T
NM_000324.3:c.-21C>T MANE Select	NP_000315.2:n.-21C>T