Canonical Allele Identifier: CA363280961
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1456354693
gnomAD v2: 6-24301979-G-A
gnomAD v4: 6-24301751-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301751G>A , CM000668.2:g.24301751G>A GRCh38
NC_000006.11:g.24301979G>A , CM000668.1:g.24301979G>A GRCh37
NC_000006.10:g.24409958G>A NCBI36
NG_012829.1:g.61302C>T
NG_012829.2:g.86542C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.521C>T MANE Select ENSP00000367715.3:p.Thr174Ile
ENST00000378454.7:c.521C>T ENSP00000367715.3:p.Thr174Ile
NM_001195610.1:c.521C>T NP_001182539.1:p.Thr174Ile
NM_016356.4:c.521C>T NP_057440.2:p.Thr174Ile
NM_016356.5:c.521C>T MANE Select NP_057440.2:p.Thr174Ile
NM_001195610.2:c.521C>T NP_001182539.1:p.Thr174Ile