Canonical Allele Identifier: CA2659494357
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831660-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831664del , CM000664.2:g.70831664del GRCh38
NC_000002.11:g.71058795del , CM000664.1:g.71058795del GRCh37
NC_000002.10:g.70912303del NCBI36
NG_033914.1:g.9163del

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+40del MANE Select ENSP00000386378.3:n.836+40del
ENST00000410009.4:c.836+40del ENSP00000386378.3:n.836+40del
NM_015717.4:c.836+40del NP_056532.4:n.836+40del
XM_011532874.1:c.836+40del XP_011531176.1:n.836+40del
XM_011532875.1:c.836+40del XP_011531177.1:n.836+40del
XM_011532876.1:c.836+40del XP_011531178.1:n.836+40del
XM_011532875.2:c.836+40del XP_011531177.1:n.836+40del
XM_011532876.2:c.836+40del XP_011531178.1:n.836+40del
NM_015717.5:c.836+40del MANE Select NP_056532.4:n.836+40del
Search 100 bp 5'
Search 100 bp 3'