Canonical Allele Identifier: CA136637348
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1027723898
gnomAD v2: 6-24302376-T-C
gnomAD v3: 6-24302148-T-C
gnomAD v4: 6-24302148-T-C
MyVariant Identifiers: chr6:g.24302376T>C (hg19) chr6:g.24302148T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24302148T>C , CM000668.2:g.24302148T>C GRCh38
NC_000006.11:g.24302376T>C , CM000668.1:g.24302376T>C GRCh37
NC_000006.10:g.24410355T>C NCBI36
NG_012829.1:g.60905A>G
NG_012829.2:g.86145A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.349-104A>G MANE Select ENSP00000367715.3:n.349-104A>G
ENST00000378454.7:c.349-104A>G ENSP00000367715.3:n.349-104A>G
NM_001195610.1:c.349-104A>G NP_001182539.1:n.349-104A>G
NM_016356.4:c.349-104A>G NP_057440.2:n.349-104A>G
NM_016356.5:c.349-104A>G MANE Select NP_057440.2:n.349-104A>G
NM_001195610.2:c.349-104A>G NP_001182539.1:n.349-104A>G
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