Canonical Allele Identifier: CA12408111

Gene: DCDC2

Linked Data

• dbSNP Id: rs147064489
• gnomAD v2: 6-24207128-T-G
• gnomAD v3: 6-24206900-T-G
• gnomAD v4: 6-24206900-T-G
• MyVariant Identifiers: chr6:g.24207128T>G (hg19) ; chr6:g.24206900T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24206900T>G , CM000668.2:g.24206900T>G	GRCh38
NC_000006.11:g.24207128T>G , CM000668.1:g.24207128T>G	GRCh37
NC_000006.10:g.24315107T>G	NCBI36
NG_012829.1:g.156153A>C
NG_012829.2:g.181393A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.923-1798A>C MANE Select	ENSP00000367715.3:n.923-1798A>C
ENST00000378454.7:c.923-1798A>C	ENSP00000367715.3:n.923-1798A>C
NM_001195610.1:c.923-1798A>C	NP_001182539.1:n.923-1798A>C
NM_016356.4:c.923-1798A>C	NP_057440.2:n.923-1798A>C
NM_016356.5:c.923-1798A>C MANE Select	NP_057440.2:n.923-1798A>C
NM_001195610.2:c.923-1798A>C	NP_001182539.1:n.923-1798A>C