Canonical Allele Identifier: CA402135326
Gene: DSG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.29104549G>C (hg19) chr18:g.31524586G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31524586G>C , CM000680.2:g.31524586G>C GRCh38
NC_000018.9:g.29104549G>C , CM000680.1:g.29104549G>C GRCh37
NC_000018.8:g.27358547G>C NCBI36
NG_007072.3:g.31345G>C , LRG_397:g.31345G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682087.2:n.659+1G>C
ENST00000683614.2:n.659+1G>C
ENST00000682087.1:c.659+1G>C
ENST00000683614.1:c.659+1G>C
ENST00000261590.13:c.828+1G>C MANE Select ENSP00000261590.8:n.828+1G>C
ENST00000261590.12:c.828+1G>C ENSP00000261590.8:n.828+1G>C
NM_001943.3:c.828+1G>C , LRG_397t1:c.828+1G>C NP_001934.2:n.828+1G>C
NM_001943.4:c.828+1G>C NP_001934.2:n.828+1G>C
XM_024451095.1:c.294+1G>C XP_024306863.1:n.294+1G>C
NM_001943.5:c.828+1G>C MANE Select NP_001934.2:n.828+1G>C
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