Canonical Allele Identifier: CA347179471
Gene: CD207 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831754T>G , CM000664.2:g.70831754T>G GRCh38
NC_000002.11:g.71058885T>G , CM000664.1:g.71058885T>G GRCh37
NC_000002.10:g.70912393T>G NCBI36
NG_033914.1:g.9070A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.783A>C MANE Select ENSP00000386378.3:p.Glu261Asp
ENST00000410009.4:c.783A>C ENSP00000386378.3:p.Glu261Asp
NM_015717.4:c.783A>C NP_056532.4:p.Glu261Asp
XM_011532874.1:c.783A>C XP_011531176.1:p.Glu261Asp
XM_011532875.1:c.783A>C XP_011531177.1:p.Glu261Asp
XM_011532876.1:c.783A>C XP_011531178.1:p.Glu261Asp
XM_011532875.2:c.783A>C XP_011531177.1:p.Glu261Asp
XM_011532876.2:c.783A>C XP_011531178.1:p.Glu261Asp
NM_015717.5:c.783A>C MANE Select NP_056532.4:p.Glu261Asp