Canonical Allele Identifier: CA11360581
Gene: CACNA2D2 HGNC NCBI

Linked Data

dbSNP Id: rs2236957
gnomAD v2: 3-50440426-A-G
gnomAD v3: 3-50402995-A-G
gnomAD v4: 3-50402995-A-G
MyVariant Identifiers: chr3:g.50440426A>G (hg19) chr3:g.50402995A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50402995A>G , CM000665.2:g.50402995A>G GRCh38
NC_000003.11:g.50440426A>G , CM000665.1:g.50440426A>G GRCh37
NC_000003.10:g.50415430A>G NCBI36
NG_034070.1:g.106250T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000424201.7:c.406-8827T>C MANE Select ENSP00000390329.2:n.406-8827T>C
ENST00000266039.7:c.406-8827T>C ENSP00000266039.3:n.406-8827T>C
ENST00000360963.7:c.199-8827T>C ENSP00000354228.3:n.199-8827T>C
ENST00000423994.6:c.406-8827T>C ENSP00000407393.2:n.406-8827T>C
ENST00000424201.6:c.406-8827T>C ENSP00000390329.2:n.406-8827T>C
ENST00000429770.5:c.406-8827T>C ENSP00000404631.1:n.406-8827T>C
ENST00000479441.1:c.406-8827T>C ENSP00000418081.1:n.406-8827T>C
NM_001005505.2:c.406-8827T>C NP_001005505.1:n.406-8827T>C
NM_001174051.2:c.406-8827T>C NP_001167522.1:n.406-8827T>C
NM_001291101.1:c.199-8827T>C NP_001278030.1:n.199-8827T>C
NM_006030.3:c.406-8827T>C NP_006021.2:n.406-8827T>C
XM_005265581.3:c.406-8827T>C XP_005265638.1:n.406-8827T>C
XM_011534242.1:c.406-8827T>C XP_011532544.1:n.406-8827T>C
XM_011534243.1:c.406-8827T>C XP_011532545.1:n.406-8827T>C
XM_011534244.1:c.406-8827T>C XP_011532546.1:n.406-8827T>C
XM_005265581.4:c.406-8827T>C XP_005265638.1:n.406-8827T>C
XM_011534243.2:c.406-8827T>C XP_011532545.1:n.406-8827T>C
NM_001005505.3:c.406-8827T>C NP_001005505.1:n.406-8827T>C
NM_001174051.3:c.406-8827T>C NP_001167522.1:n.406-8827T>C
NM_006030.4:c.406-8827T>C MANE Select NP_006021.2:n.406-8827T>C
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