Canonical Allele Identifier: CA1259751159
Gene: CD207 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831598G= , CM000664.2:g.70831598G= GRCh38
NC_000002.11:g.71058729G= , CM000664.1:g.71058729G= GRCh37
NC_000002.10:g.70912237G= NCBI36
NG_033914.1:g.9226C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.836+103C= MANE Select ENSP00000386378.3:n.836+103C=
ENST00000410009.4:c.836+103C= ENSP00000386378.3:n.836+103C=
NM_015717.4:c.836+103C= NP_056532.4:n.836+103C=
XM_011532874.1:c.836+103C= XP_011531176.1:n.836+103C=
XM_011532875.1:c.836+103C= XP_011531177.1:n.836+103C=
XM_011532876.1:c.836+103C= XP_011531178.1:n.836+103C=
XM_011532875.2:c.836+103C= XP_011531177.1:n.836+103C=
XM_011532876.2:c.836+103C= XP_011531178.1:n.836+103C=
NM_015717.5:c.836+103C= MANE Select NP_056532.4:n.836+103C=
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