Canonical Allele Identifier: CA1259751185
Gene: CD207 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831640C= , CM000664.2:g.70831640C= GRCh38
NC_000002.11:g.71058771C= , CM000664.1:g.71058771C= GRCh37
NC_000002.10:g.70912279C= NCBI36
NG_033914.1:g.9184G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.836+61G= MANE Select ENSP00000386378.3:n.836+61G=
ENST00000410009.4:c.836+61G= ENSP00000386378.3:n.836+61G=
NM_015717.4:c.836+61G= NP_056532.4:n.836+61G=
XM_011532874.1:c.836+61G= XP_011531176.1:n.836+61G=
XM_011532875.1:c.836+61G= XP_011531177.1:n.836+61G=
XM_011532876.1:c.836+61G= XP_011531178.1:n.836+61G=
XM_011532875.2:c.836+61G= XP_011531177.1:n.836+61G=
XM_011532876.2:c.836+61G= XP_011531178.1:n.836+61G=
NM_015717.5:c.836+61G= MANE Select NP_056532.4:n.836+61G=
Search 100 bp 5'
Search 100 bp 3'