Canonical Allele Identifier: CA3654433
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs770029938
ExAC: 6:24175018 A / C
gnomAD v2: 6-24175018-A-C
gnomAD v4: 6-24174790-A-C
MyVariant Identifiers: chr6:g.24175018A>C (hg19) chr6:g.24174790A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174790A>C , CM000668.2:g.24174790A>C GRCh38
NC_000006.11:g.24175018A>C , CM000668.1:g.24175018A>C GRCh37
NC_000006.10:g.24282997A>C NCBI36
NG_012829.1:g.188263T>G
NG_012829.2:g.213503T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1371T>G MANE Select ENSP00000367715.3:p.Ile457Met
ENST00000378450.6:c.630T>G ENSP00000367711.3:p.Ile210Met
ENST00000378454.7:c.1371T>G ENSP00000367715.3:p.Ile457Met
NM_001195610.1:c.1371T>G NP_001182539.1:p.Ile457Met
NM_016356.4:c.1371T>G NP_057440.2:p.Ile457Met
NM_016356.5:c.1371T>G MANE Select NP_057440.2:p.Ile457Met
NM_001195610.2:c.1371T>G NP_001182539.1:p.Ile457Met
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