Canonical Allele Identifier: CA347179356

Gene: CD207

Linked Data

• COSMIC: COSM1632094
• MyVariant Identifiers: chr2:g.71058836C>T (hg19) ; chr2:g.70831705C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831705C>T , CM000664.2:g.70831705C>T	GRCh38
NC_000002.11:g.71058836C>T , CM000664.1:g.71058836C>T	GRCh37
NC_000002.10:g.70912344C>T	NCBI36
NG_033914.1:g.9119G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.832G>A MANE Select	ENSP00000386378.3:p.Val278Met
ENST00000410009.4:c.832G>A	ENSP00000386378.3:p.Val278Met
NM_015717.4:c.832G>A	NP_056532.4:p.Val278Met
XM_011532874.1:c.832G>A	XP_011531176.1:p.Val278Met
XM_011532875.1:c.832G>A	XP_011531177.1:p.Val278Met
XM_011532876.1:c.832G>A	XP_011531178.1:p.Val278Met
XM_011532875.2:c.832G>A	XP_011531177.1:p.Val278Met
XM_011532876.2:c.832G>A	XP_011531178.1:p.Val278Met
NM_015717.5:c.832G>A MANE Select	NP_056532.4:p.Val278Met