Canonical Allele Identifier: CA136625869
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs746191010
gnomAD v2: 6-24207060-G-A
gnomAD v3: 6-24206832-G-A
gnomAD v4: 6-24206832-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206832G>A , CM000668.2:g.24206832G>A GRCh38
NC_000006.11:g.24207060G>A , CM000668.1:g.24207060G>A GRCh37
NC_000006.10:g.24315039G>A NCBI36
NG_012829.1:g.156221C>T
NG_012829.2:g.181461C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.923-1730C>T MANE Select ENSP00000367715.3:n.923-1730C>T
ENST00000378454.7:c.923-1730C>T ENSP00000367715.3:n.923-1730C>T
NM_001195610.1:c.923-1730C>T NP_001182539.1:n.923-1730C>T
NM_016356.4:c.923-1730C>T NP_057440.2:n.923-1730C>T
NM_016356.5:c.923-1730C>T MANE Select NP_057440.2:n.923-1730C>T
NM_001195610.2:c.923-1730C>T NP_001182539.1:n.923-1730C>T