Canonical Allele Identifier: CA363281019
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24302003C>G (hg19) chr6:g.24301775C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301775C>G , CM000668.2:g.24301775C>G GRCh38
NC_000006.11:g.24302003C>G , CM000668.1:g.24302003C>G GRCh37
NC_000006.10:g.24409982C>G NCBI36
NG_012829.1:g.61278G>C
NG_012829.2:g.86518G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.497G>C MANE Select ENSP00000367715.3:p.Trp166Ser
ENST00000378454.7:c.497G>C ENSP00000367715.3:p.Trp166Ser
NM_001195610.1:c.497G>C NP_001182539.1:p.Trp166Ser
NM_016356.4:c.497G>C NP_057440.2:p.Trp166Ser
NM_016356.5:c.497G>C MANE Select NP_057440.2:p.Trp166Ser
NM_001195610.2:c.497G>C NP_001182539.1:p.Trp166Ser
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