Canonical Allele Identifier: CA136625892
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1052126093
MyVariant Identifiers: chr6:g.24207236C>T (hg19) chr6:g.24207008C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24207008C>T , CM000668.2:g.24207008C>T GRCh38
NC_000006.11:g.24207236C>T , CM000668.1:g.24207236C>T GRCh37
NC_000006.10:g.24315215C>T NCBI36
NG_012829.1:g.156045G>A
NG_012829.2:g.181285G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1906G>A MANE Select ENSP00000367715.3:n.923-1906G>A
ENST00000378454.7:c.923-1906G>A ENSP00000367715.3:n.923-1906G>A
NM_001195610.1:c.923-1906G>A NP_001182539.1:n.923-1906G>A
NM_016356.4:c.923-1906G>A NP_057440.2:n.923-1906G>A
NM_016356.5:c.923-1906G>A MANE Select NP_057440.2:n.923-1906G>A
NM_001195610.2:c.923-1906G>A NP_001182539.1:n.923-1906G>A
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