Canonical Allele Identifier: CA318088792

Gene: CXADR

Linked Data

• dbSNP Id: rs989504960
• gnomAD v3: 21-17570113-G-C
• gnomAD v4: 21-17570113-G-C
• MyVariant Identifiers: chr21:g.18942431G>C (hg19) ; chr21:g.17570113G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.17570113G>C , CM000683.2:g.17570113G>C	GRCh38
NC_000021.8:g.18942431G>C , CM000683.1:g.18942431G>C	GRCh37
NC_000021.7:g.17864302G>C	NCBI36
NG_029458.1:g.62208G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400169.1:c.1017+4502G>C	ENSP00000383033.1:n.1017+4502G>C
NM_001207066.1:c.1017+4502G>C	NP_001193995.1:n.1017+4502G>C
XM_011529475.1:c.1017+4502G>C	XP_011527777.1:n.1017+4502G>C
XM_011529476.1:c.1017+4502G>C	XP_011527778.1:n.1017+4502G>C
XM_011529477.1:c.755+4502G>C	XP_011527779.1:n.755+4502G>C
XM_011529478.1:c.755+4502G>C	XP_011527780.1:n.755+4502G>C
XM_011529479.1:c.755+4502G>C	XP_011527781.1:n.755+4502G>C
XM_011529476.2:c.1017+4502G>C	XP_011527778.1:n.1017+4502G>C
XM_011529477.2:c.755+4502G>C	XP_011527779.1:n.755+4502G>C
XM_011529478.2:c.755+4502G>C	XP_011527780.1:n.755+4502G>C
XR_001754814.1:n.1131+4502G>C
NM_001207066.2:c.1017+4502G>C	NP_001193995.1:n.1017+4502G>C