Canonical Allele Identifier: CA448951401
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24301970-G-A
MyVariant Identifiers: chr6:g.24302198G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301970G>A , CM000668.2:g.24301970G>A GRCh38
NC_000006.11:g.24302198G>A , CM000668.1:g.24302198G>A GRCh37
NC_000006.10:g.24410177G>A NCBI36
NG_012829.1:g.61083C>T
NG_012829.2:g.86323C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.423C>T MANE Select ENSP00000367715.3:p.Ile141=
ENST00000378454.7:c.423C>T ENSP00000367715.3:p.Ile141=
NM_001195610.1:c.423C>T NP_001182539.1:p.Ile141=
NM_016356.4:c.423C>T NP_057440.2:p.Ile141=
NM_016356.5:c.423C>T MANE Select NP_057440.2:p.Ile141=
NM_001195610.2:c.423C>T NP_001182539.1:p.Ile141=
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