Canonical Allele Identifier: CA363280551
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24291249C>G (hg19) chr6:g.24291021C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24291021C>G , CM000668.2:g.24291021C>G GRCh38
NC_000006.11:g.24291249C>G , CM000668.1:g.24291249C>G GRCh37
NC_000006.10:g.24399228C>G NCBI36
NG_012829.1:g.72032G>C
NG_012829.2:g.97272G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.615G>C MANE Select ENSP00000367715.3:p.Gln205His
ENST00000378454.7:c.615G>C ENSP00000367715.3:p.Gln205His
NM_001195610.1:c.615G>C NP_001182539.1:p.Gln205His
NM_016356.4:c.615G>C NP_057440.2:p.Gln205His
NM_016356.5:c.615G>C MANE Select NP_057440.2:p.Gln205His
NM_001195610.2:c.615G>C NP_001182539.1:p.Gln205His
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