Canonical Allele Identifier: CA1259751191
Gene: CD207 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831656T= , CM000664.2:g.70831656T= GRCh38
NC_000002.11:g.71058787T= , CM000664.1:g.71058787T= GRCh37
NC_000002.10:g.70912295T= NCBI36
NG_033914.1:g.9168A=

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+45A= MANE Select ENSP00000386378.3:n.836+45A=
ENST00000410009.4:c.836+45A= ENSP00000386378.3:n.836+45A=
NM_015717.4:c.836+45A= NP_056532.4:n.836+45A=
XM_011532874.1:c.836+45A= XP_011531176.1:n.836+45A=
XM_011532875.1:c.836+45A= XP_011531177.1:n.836+45A=
XM_011532876.1:c.836+45A= XP_011531178.1:n.836+45A=
XM_011532875.2:c.836+45A= XP_011531177.1:n.836+45A=
XM_011532876.2:c.836+45A= XP_011531178.1:n.836+45A=
NM_015717.5:c.836+45A= MANE Select NP_056532.4:n.836+45A=