Canonical Allele Identifier: CA1616387182
Gene: DCDC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24209053C= , CM000668.2:g.24209053C= GRCh38
NC_000006.11:g.24209281C= , CM000668.1:g.24209281C= GRCh37
NC_000006.10:g.24317260C= NCBI36
NG_012829.1:g.154000G=
NG_012829.2:g.179240G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-3951G= MANE Select ENSP00000367715.3:n.923-3951G=
ENST00000378454.7:c.923-3951G= ENSP00000367715.3:n.923-3951G=
NM_001195610.1:c.923-3951G= NP_001182539.1:n.923-3951G=
NM_016356.4:c.923-3951G= NP_057440.2:n.923-3951G=
NM_016356.5:c.923-3951G= MANE Select NP_057440.2:n.923-3951G=
NM_001195610.2:c.923-3951G= NP_001182539.1:n.923-3951G=
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