Canonical Allele Identifier: CA426673142

Gene: CD207

Linked Data

• MyVariant Identifiers: chr2:g.71058855T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831724T>A , CM000664.2:g.70831724T>A	GRCh38
NC_000002.11:g.71058855T>A , CM000664.1:g.71058855T>A	GRCh37
NC_000002.10:g.70912363T>A	NCBI36
NG_033914.1:g.9100A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.813A>T MANE Select	ENSP00000386378.3:p.Pro271=
ENST00000410009.4:c.813A>T	ENSP00000386378.3:p.Pro271=
NM_015717.4:c.813A>T	NP_056532.4:p.Pro271=
XM_011532874.1:c.813A>T	XP_011531176.1:p.Pro271=
XM_011532875.1:c.813A>T	XP_011531177.1:p.Pro271=
XM_011532876.1:c.813A>T	XP_011531178.1:p.Pro271=
XM_011532875.2:c.813A>T	XP_011531177.1:p.Pro271=
XM_011532876.2:c.813A>T	XP_011531178.1:p.Pro271=
NM_015717.5:c.813A>T MANE Select	NP_056532.4:p.Pro271=