Canonical Allele Identifier: CA500989326
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069085G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991721G>C , CM000679.2:g.49991721G>C GRCh38
NC_000017.10:g.48069085G>C , CM000679.1:g.48069085G>C GRCh37
NC_000017.9:g.45424084G>C NCBI36
NG_023063.1:g.8504C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.660C>G MANE Select ENSP00000389870.2:p.Ser220=
ENST00000512495.2:c.300C>G ENSP00000449976.1:p.Ser100=
NM_005220.2:c.660C>G NP_005211.1:p.Ser220=
XM_011524458.1:c.516+1679C>G XP_011522760.1:n.516+1679C>G
NM_005220.3:c.660C>G MANE Select NP_005211.1:p.Ser220=
Search 100 bp 5'
Search 100 bp 3'