Canonical Allele Identifier: CA347179622

Gene: CD207

Linked Data

• dbSNP Id: rs1384052006
• gnomAD v3: 2-70831820-C-T
• gnomAD v4: 2-70831820-C-T
• MyVariant Identifiers: chr2:g.71058951C>T (hg19) ; chr2:g.70831820C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831820C>T , CM000664.2:g.70831820C>T	GRCh38
NC_000002.11:g.71058951C>T , CM000664.1:g.71058951C>T	GRCh37
NC_000002.10:g.70912459C>T	NCBI36
NG_033914.1:g.9004G>A

Transcript Alleles

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