Canonical Allele Identifier: CA1259751287

Gene: CD207

Linked Data

• dbSNP Id: rs372110264

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831860G>C , CM000664.2:g.70831860G>C	GRCh38
NC_000002.11:g.71058991G>C , CM000664.1:g.71058991G>C	GRCh37
NC_000002.10:g.70912499G>C	NCBI36
NG_033914.1:g.8964C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-41C>G MANE Select	ENSP00000386378.3:n.718-41C>G
ENST00000410009.4:c.718-41C>G	ENSP00000386378.3:n.718-41C>G
NM_015717.4:c.718-41C>G	NP_056532.4:n.718-41C>G
XM_011532874.1:c.718-41C>G	XP_011531176.1:n.718-41C>G
XM_011532875.1:c.718-41C>G	XP_011531177.1:n.718-41C>G
XM_011532876.1:c.718-41C>G	XP_011531178.1:n.718-41C>G
XM_011532875.2:c.718-41C>G	XP_011531177.1:n.718-41C>G
XM_011532876.2:c.718-41C>G	XP_011531178.1:n.718-41C>G
NM_015717.5:c.718-41C>G MANE Select	NP_056532.4:n.718-41C>G