Canonical Allele Identifier: CA347179465

Gene: CD207

Linked Data

• MyVariant Identifiers: chr2:g.71058883C>A (hg19) ; chr2:g.70831752C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831752C>A , CM000664.2:g.70831752C>A	GRCh38
NC_000002.11:g.71058883C>A , CM000664.1:g.71058883C>A	GRCh37
NC_000002.10:g.70912391C>A	NCBI36
NG_033914.1:g.9072G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000410009.5:c.785G>T MANE Select	ENSP00000386378.3:p.Gly262Val
ENST00000410009.4:c.785G>T	ENSP00000386378.3:p.Gly262Val
NM_015717.4:c.785G>T	NP_056532.4:p.Gly262Val
XM_011532874.1:c.785G>T	XP_011531176.1:p.Gly262Val
XM_011532875.1:c.785G>T	XP_011531177.1:p.Gly262Val
XM_011532876.1:c.785G>T	XP_011531178.1:p.Gly262Val
XM_011532875.2:c.785G>T	XP_011531177.1:p.Gly262Val
XM_011532876.2:c.785G>T	XP_011531178.1:p.Gly262Val
NM_015717.5:c.785G>T MANE Select	NP_056532.4:p.Gly262Val