Canonical Allele Identifier: CA448951379
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24301810-A-G
MyVariant Identifiers: chr6:g.24302038A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301810A>G , CM000668.2:g.24301810A>G GRCh38
NC_000006.11:g.24302038A>G , CM000668.1:g.24302038A>G GRCh37
NC_000006.10:g.24410017A>G NCBI36
NG_012829.1:g.61243T>C
NG_012829.2:g.86483T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.462T>C MANE Select ENSP00000367715.3:p.Ser154=
ENST00000378454.7:c.462T>C ENSP00000367715.3:p.Ser154=
NM_001195610.1:c.462T>C NP_001182539.1:p.Ser154=
NM_016356.4:c.462T>C NP_057440.2:p.Ser154=
NM_016356.5:c.462T>C MANE Select NP_057440.2:p.Ser154=
NM_001195610.2:c.462T>C NP_001182539.1:p.Ser154=
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