Canonical Allele Identifier: CA16309846
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 674180
ClinVar RCV Id: RCV000833491
dbSNP Id: rs362719
gnomAD v2: 7-103185877-C-A
gnomAD v3: 7-103545430-C-A
gnomAD v4: 7-103545430-C-A
MyVariant Identifiers: chr7:g.103185877C>A (hg19) chr7:g.103545430C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.103545430C>A , CM000669.2:g.103545430C>A GRCh38
NC_000007.13:g.103185877C>A , CM000669.1:g.103185877C>A GRCh37
NC_000007.12:g.102973113C>A NCBI36
NG_011877.1:g.449087G>T
NG_011877.2:g.449087G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000424685.3:c.6303-86G>T ENSP00000388446.3:n.6303-86G>T
ENST00000428762.6:c.6303-86G>T MANE Select ENSP00000392423.1:n.6303-86G>T
ENST00000679867.1:n.6187-86G>T
ENST00000679952.1:n.95-86G>T
ENST00000681034.1:c.6303-86G>T ENSP00000506075.1:n.6303-86G>T
ENST00000681199.1:n.2071-86G>T
ENST00000343529.9:c.6303-86G>T ENSP00000345694.5:n.6303-86G>T
ENST00000424685.2:c.6303-86G>T ENSP00000388446.2:n.6303-86G>T
ENST00000428762.5:c.6303-86G>T ENSP00000392423.1:n.6303-86G>T
NM_005045.3:c.6303-86G>T NP_005036.2:n.6303-86G>T
NM_173054.2:c.6303-86G>T NP_774959.1:n.6303-86G>T
NM_005045.4:c.6303-86G>T MANE Select NP_005036.2:n.6303-86G>T
NM_173054.3:c.6303-86G>T NP_774959.1:n.6303-86G>T
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