Canonical Allele Identifier: CA988919048

Gene: DSG2

Linked Data

• dbSNP Id: rs2073115642
• gnomAD v3: 18-31519672-A-C
• gnomAD v4: 18-31519672-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31519672A>C , CM000680.2:g.31519672A>C	GRCh38
NC_000018.9:g.29099635A>C , CM000680.1:g.29099635A>C	GRCh37
NC_000018.8:g.27353633A>C	NCBI36
NG_007072.3:g.26431A>C , LRG_397:g.26431A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682241.2:c.82-131A>C	ENSP00000507600.2:n.82-131A>C
ENST00000683654.1:c.82-131A>C	ENSP00000506971.1:n.82-131A>C
ENST00000261590.13:c.82-131A>C MANE Select	ENSP00000261590.8:n.82-131A>C
ENST00000261590.12:c.82-131A>C	ENSP00000261590.8:n.82-131A>C
ENST00000585206.1:c.82-131A>C	ENSP00000462503.1:n.82-131A>C
NM_001943.3:c.82-131A>C , LRG_397t1:c.82-131A>C	NP_001934.2:n.82-131A>C
NM_001943.4:c.82-131A>C	NP_001934.2:n.82-131A>C
XM_024451095.1:c.-453-131A>C	XP_024306863.1:n.-453-131A>C
NM_001943.5:c.82-131A>C MANE Select	NP_001934.2:n.82-131A>C