Canonical Allele Identifier: CA136634488
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs807725
gnomAD v2: 6-24278770-A-G
gnomAD v3: 6-24278542-A-G
gnomAD v4: 6-24278542-A-G
MyVariant Identifiers: chr6:g.24278770A>G (hg19) chr6:g.24278542A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278542A>G , CM000668.2:g.24278542A>G GRCh38
NC_000006.11:g.24278770A>G , CM000668.1:g.24278770A>G GRCh37
NC_000006.10:g.24386749A>G NCBI36
NG_012829.1:g.84511T>C
NG_012829.2:g.109751T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-331T>C MANE Select ENSP00000367715.3:n.760-331T>C
ENST00000378454.7:c.760-331T>C ENSP00000367715.3:n.760-331T>C
NM_001195610.1:c.760-331T>C NP_001182539.1:n.760-331T>C
NM_016356.4:c.760-331T>C NP_057440.2:n.760-331T>C
NM_016356.5:c.760-331T>C MANE Select NP_057440.2:n.760-331T>C
NM_001195610.2:c.760-331T>C NP_001182539.1:n.760-331T>C
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