Canonical Allele Identifier: CA892614695
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1442967629
MyVariant Identifiers: chr2:g.70832035del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70832036del , CM000664.2:g.70832036del GRCh38
NC_000002.11:g.71059167del , CM000664.1:g.71059167del GRCh37
NC_000002.10:g.70912675del NCBI36
NG_033914.1:g.8789del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-216del MANE Select ENSP00000386378.3:n.718-216del
ENST00000410009.4:c.718-216del ENSP00000386378.3:n.718-216del
NM_015717.4:c.718-216del NP_056532.4:n.718-216del
XM_011532874.1:c.718-216del XP_011531176.1:n.718-216del
XM_011532875.1:c.718-216del XP_011531177.1:n.718-216del
XM_011532876.1:c.718-216del XP_011531178.1:n.718-216del
XM_011532875.2:c.718-216del XP_011531177.1:n.718-216del
XM_011532876.2:c.718-216del XP_011531178.1:n.718-216del
NM_015717.5:c.718-216del MANE Select NP_056532.4:n.718-216del
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