Canonical Allele Identifier: CA2641407009

Gene: DSG2

Linked Data

• gnomAD v4: 18-31541351-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31541351C>G , CM000680.2:g.31541351C>G	GRCh38
NC_000018.9:g.29121314C>G , CM000680.1:g.29121314C>G	GRCh37
NC_000018.8:g.27375312C>G	NCBI36
NG_007072.3:g.48110C>G , LRG_397:g.48110C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261590.13:c.2001+37C>G MANE Select	ENSP00000261590.8:n.2001+37C>G
ENST00000261590.12:c.2001+37C>G	ENSP00000261590.8:n.2001+37C>G
NM_001943.3:c.2001+37C>G , LRG_397t1:c.2001+37C>G	NP_001934.2:n.2001+37C>G
NM_001943.4:c.2001+37C>G	NP_001934.2:n.2001+37C>G
XM_024451095.1:c.1467+37C>G	XP_024306863.1:n.1467+37C>G
NM_001943.5:c.2001+37C>G MANE Select	NP_001934.2:n.2001+37C>G