Canonical Allele Identifier: CA363277438
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1380178018
MyVariant Identifiers: chr6:g.24205256T>C (hg19) chr6:g.24205028T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24205028T>C , CM000668.2:g.24205028T>C GRCh38
NC_000006.11:g.24205256T>C , CM000668.1:g.24205256T>C GRCh37
NC_000006.10:g.24313235T>C NCBI36
NG_012829.1:g.158025A>G
NG_012829.2:g.183265A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.997A>G MANE Select ENSP00000367715.3:p.Thr333Ala
ENST00000378450.6:c.256A>G ENSP00000367711.3:p.Thr86Ala
ENST00000378454.7:c.997A>G ENSP00000367715.3:p.Thr333Ala
NM_001195610.1:c.997A>G NP_001182539.1:p.Thr333Ala
NM_016356.4:c.997A>G NP_057440.2:p.Thr333Ala
NM_016356.5:c.997A>G MANE Select NP_057440.2:p.Thr333Ala
NM_001195610.2:c.997A>G NP_001182539.1:p.Thr333Ala
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