Canonical Allele Identifier: CA426673183

Gene: CD207

Linked Data

• MyVariant Identifiers: chr2:g.71058921G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831790G>C , CM000664.2:g.70831790G>C	GRCh38
NC_000002.11:g.71058921G>C , CM000664.1:g.71058921G>C	GRCh37
NC_000002.10:g.70912429G>C	NCBI36
NG_033914.1:g.9034C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.747C>G MANE Select	ENSP00000386378.3:p.Leu249=
ENST00000410009.4:c.747C>G	ENSP00000386378.3:p.Leu249=
NM_015717.4:c.747C>G	NP_056532.4:p.Leu249=
XM_011532874.1:c.747C>G	XP_011531176.1:p.Leu249=
XM_011532875.1:c.747C>G	XP_011531177.1:p.Leu249=
XM_011532876.1:c.747C>G	XP_011531178.1:p.Leu249=
XM_011532875.2:c.747C>G	XP_011531177.1:p.Leu249=
XM_011532876.2:c.747C>G	XP_011531178.1:p.Leu249=
NM_015717.5:c.747C>G MANE Select	NP_056532.4:p.Leu249=