Canonical Allele Identifier: CA347179441
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831741-A-G
MyVariant Identifiers: chr2:g.71058872A>G (hg19) chr2:g.70831741A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831741A>G , CM000664.2:g.70831741A>G GRCh38
NC_000002.11:g.71058872A>G , CM000664.1:g.71058872A>G GRCh37
NC_000002.10:g.70912380A>G NCBI36
NG_033914.1:g.9083T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.796T>C MANE Select ENSP00000386378.3:p.Trp266Arg
ENST00000410009.4:c.796T>C ENSP00000386378.3:p.Trp266Arg
NM_015717.4:c.796T>C NP_056532.4:p.Trp266Arg
XM_011532874.1:c.796T>C XP_011531176.1:p.Trp266Arg
XM_011532875.1:c.796T>C XP_011531177.1:p.Trp266Arg
XM_011532876.1:c.796T>C XP_011531178.1:p.Trp266Arg
XM_011532875.2:c.796T>C XP_011531177.1:p.Trp266Arg
XM_011532876.2:c.796T>C XP_011531178.1:p.Trp266Arg
NM_015717.5:c.796T>C MANE Select NP_056532.4:p.Trp266Arg
Search 100 bp 5'
Search 100 bp 3'