Canonical Allele Identifier: CA347179522

Gene: CD207

Linked Data

• MyVariant Identifiers: chr2:g.71058907C>T (hg19) ; chr2:g.70831776C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831776C>T , CM000664.2:g.70831776C>T	GRCh38
NC_000002.11:g.71058907C>T , CM000664.1:g.71058907C>T	GRCh37
NC_000002.10:g.70912415C>T	NCBI36
NG_033914.1:g.9048G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.761G>A MANE Select	ENSP00000386378.3:p.Gly254Asp
ENST00000410009.4:c.761G>A	ENSP00000386378.3:p.Gly254Asp
NM_015717.4:c.761G>A	NP_056532.4:p.Gly254Asp
XM_011532874.1:c.761G>A	XP_011531176.1:p.Gly254Asp
XM_011532875.1:c.761G>A	XP_011531177.1:p.Gly254Asp
XM_011532876.1:c.761G>A	XP_011531178.1:p.Gly254Asp
XM_011532875.2:c.761G>A	XP_011531177.1:p.Gly254Asp
XM_011532876.2:c.761G>A	XP_011531178.1:p.Gly254Asp
NM_015717.5:c.761G>A MANE Select	NP_056532.4:p.Gly254Asp