Canonical Allele Identifier: CA13126550
Gene: DEC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10817758

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.115381654C>T , CM000671.2:g.115381654C>T GRCh38
NC_000009.11:g.118143933C>T , CM000671.1:g.118143933C>T GRCh37
NC_000009.10:g.117183754C>T NCBI36
NG_027530.1:g.244837C>T

Transcript Alleles

HGVS Amino-acid change
NM_017418.2:c.13+4939C>T VV NP_059114.1:p.=
XM_011518753.1:c.13+4939C>T XP_011517055.1:p.=
ENST00000374016.5:c.13+4939C>T ENSP00000363128.1:p.=