Canonical Allele Identifier: CA1259751348

Gene: CD207

Linked Data

• dbSNP Id: rs1677486783

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831971A>T , CM000664.2:g.70831971A>T	GRCh38
NC_000002.11:g.71059102A>T , CM000664.1:g.71059102A>T	GRCh37
NC_000002.10:g.70912610A>T	NCBI36
NG_033914.1:g.8853T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-152T>A MANE Select	ENSP00000386378.3:n.718-152T>A
ENST00000410009.4:c.718-152T>A	ENSP00000386378.3:n.718-152T>A
NM_015717.4:c.718-152T>A	NP_056532.4:n.718-152T>A
XM_011532874.1:c.718-152T>A	XP_011531176.1:n.718-152T>A
XM_011532875.1:c.718-152T>A	XP_011531177.1:n.718-152T>A
XM_011532876.1:c.718-152T>A	XP_011531178.1:n.718-152T>A
XM_011532875.2:c.718-152T>A	XP_011531177.1:n.718-152T>A
XM_011532876.2:c.718-152T>A	XP_011531178.1:n.718-152T>A
NM_015717.5:c.718-152T>A MANE Select	NP_056532.4:n.718-152T>A