Canonical Allele Identifier: CA347179549

Gene: CD207

Linked Data

• MyVariant Identifiers: chr2:g.71058917A>T (hg19) ; chr2:g.70831786A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831786A>T , CM000664.2:g.70831786A>T	GRCh38
NC_000002.11:g.71058917A>T , CM000664.1:g.71058917A>T	GRCh37
NC_000002.10:g.70912425A>T	NCBI36
NG_033914.1:g.9038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.751T>A MANE Select	ENSP00000386378.3:p.Tyr251Asn
ENST00000410009.4:c.751T>A	ENSP00000386378.3:p.Tyr251Asn
NM_015717.4:c.751T>A	NP_056532.4:p.Tyr251Asn
XM_011532874.1:c.751T>A	XP_011531176.1:p.Tyr251Asn
XM_011532875.1:c.751T>A	XP_011531177.1:p.Tyr251Asn
XM_011532876.1:c.751T>A	XP_011531178.1:p.Tyr251Asn
XM_011532875.2:c.751T>A	XP_011531177.1:p.Tyr251Asn
XM_011532876.2:c.751T>A	XP_011531178.1:p.Tyr251Asn
NM_015717.5:c.751T>A MANE Select	NP_056532.4:p.Tyr251Asn