Canonical Allele Identifier: CA448951183
Gene: DCDC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.24291207A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290979A>C , CM000668.2:g.24290979A>C GRCh38
NC_000006.11:g.24291207A>C , CM000668.1:g.24291207A>C GRCh37
NC_000006.10:g.24399186A>C NCBI36
NG_012829.1:g.72074T>G
NG_012829.2:g.97314T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.657T>G MANE Select ENSP00000367715.3:p.Pro219=
ENST00000378454.7:c.657T>G ENSP00000367715.3:p.Pro219=
NM_001195610.1:c.657T>G NP_001182539.1:p.Pro219=
NM_016356.4:c.657T>G NP_057440.2:p.Pro219=
NM_016356.5:c.657T>G MANE Select NP_057440.2:p.Pro219=
NM_001195610.2:c.657T>G NP_001182539.1:p.Pro219=