Canonical Allele Identifier: CA363280239
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1763729598
MyVariant Identifiers: chr6:g.24291184T>A (hg19) chr6:g.24290956T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290956T>A , CM000668.2:g.24290956T>A GRCh38
NC_000006.11:g.24291184T>A , CM000668.1:g.24291184T>A GRCh37
NC_000006.10:g.24399163T>A NCBI36
NG_012829.1:g.72097A>T
NG_012829.2:g.97337A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.680A>T MANE Select ENSP00000367715.3:p.Lys227Met
ENST00000378454.7:c.680A>T ENSP00000367715.3:p.Lys227Met
NM_001195610.1:c.680A>T NP_001182539.1:p.Lys227Met
NM_016356.4:c.680A>T NP_057440.2:p.Lys227Met
NM_016356.5:c.680A>T MANE Select NP_057440.2:p.Lys227Met
NM_001195610.2:c.680A>T NP_001182539.1:p.Lys227Met
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