Canonical Allele Identifier: CA1616386101
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206892T>C , CM000668.2:g.24206892T>C GRCh38
NC_000006.11:g.24207120T>C , CM000668.1:g.24207120T>C GRCh37
NC_000006.10:g.24315099T>C NCBI36
NG_012829.1:g.156161A>G
NG_012829.2:g.181401A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1790A>G MANE Select ENSP00000367715.3:n.923-1790A>G
ENST00000378454.7:c.923-1790A>G ENSP00000367715.3:n.923-1790A>G
NM_001195610.1:c.923-1790A>G NP_001182539.1:n.923-1790A>G
NM_016356.4:c.923-1790A>G NP_057440.2:n.923-1790A>G
NM_016356.5:c.923-1790A>G MANE Select NP_057440.2:n.923-1790A>G
NM_001195610.2:c.923-1790A>G NP_001182539.1:n.923-1790A>G