Canonical Allele Identifier: CA2641405611
Gene: DSG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31498185G>A , CM000680.2:g.31498185G>A GRCh38
NC_000018.9:g.29078148G>A , CM000680.1:g.29078148G>A GRCh37
NC_000018.8:g.27332146G>A NCBI36
NG_007072.3:g.4944G>A , LRG_397:g.4944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.-67G>A MANE Select ENSP00000261590.8:n.-67G>A
ENST00000261590.12:c.-67G>A ENSP00000261590.8:n.-67G>A
NM_001943.3:c.-67G>A , LRG_397t1:c.-67G>A NP_001934.2:n.-67G>A
NM_001943.4:c.-67G>A NP_001934.2:n.-67G>A
NM_001943.5:c.-67G>A MANE Select NP_001934.2:n.-67G>A