Canonical Allele Identifier: CA154928
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 130133
ClinVar RCV Id: RCV000118162 RCV000290302 RCV000513733 RCV001082701 RCV001252608 RCV002490808
dbSNP Id: rs116716038
ExAC: 7:103185751 C / T
gnomAD v2: 7-103185751-C-T
gnomAD v3: 7-103545304-C-T
gnomAD v4: 7-103545304-C-T
COSMIC: COSM1581589
MyVariant Identifiers: chr7:g.103185751C>T (hg19) chr7:g.103545304C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103545304C>T , CM000669.2:g.103545304C>T GRCh38
NC_000007.13:g.103185751C>T , CM000669.1:g.103185751C>T GRCh37
NC_000007.12:g.102972987C>T NCBI36
NG_011877.1:g.449213G>A
NG_011877.2:g.449213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000424685.3:c.6343G>A ENSP00000388446.3:p.Gly2115Ser
ENST00000428762.6:c.6343G>A MANE Select ENSP00000392423.1:p.Gly2115Ser
ENST00000679867.1:n.6227G>A
ENST00000679952.1:n.135G>A
ENST00000681034.1:c.6343G>A ENSP00000506075.1:p.Gly2115Ser
ENST00000681199.1:n.2111G>A
ENST00000343529.9:c.6343G>A ENSP00000345694.5:p.Gly2115Ser
ENST00000424685.2:c.6343G>A ENSP00000388446.2:p.Gly2115Ser
ENST00000428762.5:c.6343G>A ENSP00000392423.1:p.Gly2115Ser
NM_005045.3:c.6343G>A NP_005036.2:p.Gly2115Ser
NM_173054.2:c.6343G>A NP_774959.1:p.Gly2115Ser
NM_005045.4:c.6343G>A MANE Select NP_005036.2:p.Gly2115Ser
NM_173054.3:c.6343G>A NP_774959.1:p.Gly2115Ser
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