Canonical Allele Identifier: CA503766598
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

gnomAD v4: 18-31546515-T-C
MyVariant Identifiers: chr18:g.29126478T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546515T>C , CM000680.2:g.31546515T>C GRCh38
NC_000018.9:g.29126478T>C , CM000680.1:g.29126478T>C GRCh37
NC_000018.8:g.27380476T>C NCBI36
NG_007072.3:g.53274T>C , LRG_397:g.53274T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3129T>C (DSG2) MANE Select ENSP00000261590.8:p.Asn1043=
ENST00000261590.12:c.3129T>C (DSG2) ENSP00000261590.8:p.Asn1043=
NM_001943.3:c.3129T>C , LRG_397t1:c.3129T>C (DSG2) NP_001934.2:p.Asn1043=
NR_045216.1:n.1346-609A>G (DSG2-AS1)
NM_001943.4:c.3129T>C (DSG2) NP_001934.2:p.Asn1043=
XM_024451095.1:c.2595T>C (DSG2) XP_024306863.1:p.Asn865=
NM_001943.5:c.3129T>C (DSG2) MANE Select NP_001934.2:p.Asn1043=
Search 100 bp 5'
Search 100 bp 3'