Canonical Allele Identifier: CA2838812156
Gene: DSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31541345C>G , CM000680.2:g.31541345C>G GRCh38
NC_000018.9:g.29121308C>G , CM000680.1:g.29121308C>G GRCh37
NC_000018.8:g.27375306C>G NCBI36
NG_007072.3:g.48104C>G , LRG_397:g.48104C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2001+31C>G MANE Select ENSP00000261590.8:n.2001+31C>G
ENST00000261590.12:c.2001+31C>G ENSP00000261590.8:n.2001+31C>G
NM_001943.3:c.2001+31C>G , LRG_397t1:c.2001+31C>G NP_001934.2:n.2001+31C>G
NM_001943.4:c.2001+31C>G NP_001934.2:n.2001+31C>G
XM_024451095.1:c.1467+31C>G XP_024306863.1:n.1467+31C>G
NM_001943.5:c.2001+31C>G MANE Select NP_001934.2:n.2001+31C>G