Canonical Allele Identifier: CA3654752
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs767941715
ExAC: 6:24302054 A / G
gnomAD v2: 6-24302054-A-G
gnomAD v4: 6-24301826-A-G
MyVariant Identifiers: chr6:g.24302054A>G (hg19) chr6:g.24301826A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301826A>G , CM000668.2:g.24301826A>G GRCh38
NC_000006.11:g.24302054A>G , CM000668.1:g.24302054A>G GRCh37
NC_000006.10:g.24410033A>G NCBI36
NG_012829.1:g.61227T>C
NG_012829.2:g.86467T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.446T>C MANE Select ENSP00000367715.3:p.Leu149Pro
ENST00000378454.7:c.446T>C ENSP00000367715.3:p.Leu149Pro
NM_001195610.1:c.446T>C NP_001182539.1:p.Leu149Pro
NM_016356.4:c.446T>C NP_057440.2:p.Leu149Pro
NM_016356.5:c.446T>C MANE Select NP_057440.2:p.Leu149Pro
NM_001195610.2:c.446T>C NP_001182539.1:p.Leu149Pro
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