Canonical Allele Identifier: CA892614689

Gene: CD207

Linked Data

• dbSNP Id: rs1273814384
• MyVariant Identifiers: chr2:g.70832015A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70832015A>C , CM000664.2:g.70832015A>C	GRCh38
NC_000002.11:g.71059146A>C , CM000664.1:g.71059146A>C	GRCh37
NC_000002.10:g.70912654A>C	NCBI36
NG_033914.1:g.8809T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-196T>G MANE Select	ENSP00000386378.3:n.718-196T>G
ENST00000410009.4:c.718-196T>G	ENSP00000386378.3:n.718-196T>G
NM_015717.4:c.718-196T>G	NP_056532.4:n.718-196T>G
XM_011532874.1:c.718-196T>G	XP_011531176.1:n.718-196T>G
XM_011532875.1:c.718-196T>G	XP_011531177.1:n.718-196T>G
XM_011532876.1:c.718-196T>G	XP_011531178.1:n.718-196T>G
XM_011532875.2:c.718-196T>G	XP_011531177.1:n.718-196T>G
XM_011532876.2:c.718-196T>G	XP_011531178.1:n.718-196T>G
NM_015717.5:c.718-196T>G MANE Select	NP_056532.4:n.718-196T>G