Canonical Allele Identifier: CA1032026375
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1677484636
gnomAD v3: 2-70831899-CT-C
gnomAD v4: 2-70831899-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831900del , CM000664.2:g.70831900del GRCh38
NC_000002.11:g.71059031del , CM000664.1:g.71059031del GRCh37
NC_000002.10:g.70912539del NCBI36
NG_033914.1:g.8924del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-81del MANE Select ENSP00000386378.3:n.718-81del
ENST00000410009.4:c.718-81del ENSP00000386378.3:n.718-81del
NM_015717.4:c.718-81del NP_056532.4:n.718-81del
XM_011532874.1:c.718-81del XP_011531176.1:n.718-81del
XM_011532875.1:c.718-81del XP_011531177.1:n.718-81del
XM_011532876.1:c.718-81del XP_011531178.1:n.718-81del
XM_011532875.2:c.718-81del XP_011531177.1:n.718-81del
XM_011532876.2:c.718-81del XP_011531178.1:n.718-81del
NM_015717.5:c.718-81del MANE Select NP_056532.4:n.718-81del
Search 100 bp 5'
Search 100 bp 3'