Canonical Allele Identifier: CA448951341
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24301741-G-A
MyVariant Identifiers: chr6:g.24301969G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301741G>A , CM000668.2:g.24301741G>A GRCh38
NC_000006.11:g.24301969G>A , CM000668.1:g.24301969G>A GRCh37
NC_000006.10:g.24409948G>A NCBI36
NG_012829.1:g.61312C>T
NG_012829.2:g.86552C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.531C>T MANE Select ENSP00000367715.3:p.Ile177=
ENST00000378454.7:c.531C>T ENSP00000367715.3:p.Ile177=
NM_001195610.1:c.531C>T NP_001182539.1:p.Ile177=
NM_016356.4:c.531C>T NP_057440.2:p.Ile177=
NM_016356.5:c.531C>T MANE Select NP_057440.2:p.Ile177=
NM_001195610.2:c.531C>T NP_001182539.1:p.Ile177=