Canonical Allele Identifier: CA448951346
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1180457464
MyVariant Identifiers: chr6:g.24301981G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301753G>A , CM000668.2:g.24301753G>A GRCh38
NC_000006.11:g.24301981G>A , CM000668.1:g.24301981G>A GRCh37
NC_000006.10:g.24409960G>A NCBI36
NG_012829.1:g.61300C>T
NG_012829.2:g.86540C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.519C>T MANE Select ENSP00000367715.3:p.Val173=
ENST00000378454.7:c.519C>T ENSP00000367715.3:p.Val173=
NM_001195610.1:c.519C>T NP_001182539.1:p.Val173=
NM_016356.4:c.519C>T NP_057440.2:p.Val173=
NM_016356.5:c.519C>T MANE Select NP_057440.2:p.Val173=
NM_001195610.2:c.519C>T NP_001182539.1:p.Val173=