Canonical Allele Identifier: CA566224231
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1199336202
gnomAD v2: 6-24348059-G-A
gnomAD v3: 6-24347831-G-A
gnomAD v4: 6-24347831-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347831G>A , CM000668.2:g.24347831G>A GRCh38
NC_000006.11:g.24348059G>A , CM000668.1:g.24348059G>A GRCh37
NC_000006.10:g.24456038G>A NCBI36
NG_012829.1:g.15222C>T
NG_012829.2:g.40462C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5738C>T MANE Select ENSP00000367715.3:n.348+5738C>T
ENST00000378454.7:c.348+5738C>T ENSP00000367715.3:n.348+5738C>T
NM_001195610.1:c.348+5738C>T NP_001182539.1:n.348+5738C>T
NM_016356.4:c.348+5738C>T NP_057440.2:n.348+5738C>T
NM_016356.5:c.348+5738C>T MANE Select NP_057440.2:n.348+5738C>T
NM_001195610.2:c.348+5738C>T NP_001182539.1:n.348+5738C>T