Canonical Allele Identifier: CA136637332

Gene: DCDC2

Linked Data

• dbSNP Id: rs766909616
• gnomAD v4: 6-24301941-C-G
• MyVariant Identifiers: chr6:g.24301941C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24301941C>G , CM000668.2:g.24301941C>G	GRCh38
NC_000006.11:g.24302169C>G , CM000668.1:g.24302169C>G	GRCh37
NC_000006.10:g.24410148C>G	NCBI36
NG_012829.1:g.61112G>C
NG_012829.2:g.86352G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.425+27G>C MANE Select	ENSP00000367715.3:n.425+27G>C
ENST00000378454.7:c.425+27G>C	ENSP00000367715.3:n.425+27G>C
NM_001195610.1:c.425+27G>C	NP_001182539.1:n.425+27G>C
NM_016356.4:c.425+27G>C	NP_057440.2:n.425+27G>C
NM_016356.5:c.425+27G>C MANE Select	NP_057440.2:n.425+27G>C
NM_001195610.2:c.425+27G>C	NP_001182539.1:n.425+27G>C