Canonical Allele Identifier: CA2576996709

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831645T>C , CM000664.2:g.70831645T>C	GRCh38
NC_000002.11:g.71058776T>C , CM000664.1:g.71058776T>C	GRCh37
NC_000002.10:g.70912284T>C	NCBI36
NG_033914.1:g.9179A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+56A>G MANE Select	ENSP00000386378.3:n.836+56A>G
ENST00000410009.4:c.836+56A>G	ENSP00000386378.3:n.836+56A>G
NM_015717.4:c.836+56A>G	NP_056532.4:n.836+56A>G
XM_011532874.1:c.836+56A>G	XP_011531176.1:n.836+56A>G
XM_011532875.1:c.836+56A>G	XP_011531177.1:n.836+56A>G
XM_011532876.1:c.836+56A>G	XP_011531178.1:n.836+56A>G
XM_011532875.2:c.836+56A>G	XP_011531177.1:n.836+56A>G
XM_011532876.2:c.836+56A>G	XP_011531178.1:n.836+56A>G
NM_015717.5:c.836+56A>G MANE Select	NP_056532.4:n.836+56A>G