Canonical Allele Identifier: CA1616410372
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1027723898

Genomic Alleles

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

Transcript Alleles

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