Canonical Allele Identifier: CA448963068
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760972587
MyVariant Identifiers: chr6:g.24178606G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178378G>A , CM000668.2:g.24178378G>A GRCh38
NC_000006.11:g.24178606G>A , CM000668.1:g.24178606G>A GRCh37
NC_000006.10:g.24286585G>A NCBI36
NG_012829.1:g.184675C>T
NG_012829.2:g.209915C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1278C>T MANE Select ENSP00000367715.3:p.Val426=
ENST00000378450.6:c.537C>T ENSP00000367711.3:p.Val179=
ENST00000378454.7:c.1278C>T ENSP00000367715.3:p.Val426=
NM_001195610.1:c.1278C>T NP_001182539.1:p.Val426=
NM_016356.4:c.1278C>T NP_057440.2:p.Val426=
NM_016356.5:c.1278C>T MANE Select NP_057440.2:p.Val426=
NM_001195610.2:c.1278C>T NP_001182539.1:p.Val426=
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