Canonical Allele Identifier: CA448951188
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24291210C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290982C>T , CM000668.2:g.24290982C>T GRCh38
NC_000006.11:g.24291210C>T , CM000668.1:g.24291210C>T GRCh37
NC_000006.10:g.24399189C>T NCBI36
NG_012829.1:g.72071G>A
NG_012829.2:g.97311G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.654G>A MANE Select ENSP00000367715.3:p.Leu218=
ENST00000378454.7:c.654G>A ENSP00000367715.3:p.Leu218=
NM_001195610.1:c.654G>A NP_001182539.1:p.Leu218=
NM_016356.4:c.654G>A NP_057440.2:p.Leu218=
NM_016356.5:c.654G>A MANE Select NP_057440.2:p.Leu218=
NM_001195610.2:c.654G>A NP_001182539.1:p.Leu218=