Canonical Allele Identifier: CA533222145

Gene: CD207

Linked Data

• dbSNP Id: rs1553399873
• gnomAD v2: 2-71058962-A-C
• gnomAD v4: 2-70831831-A-C
• MyVariant Identifiers: chr2:g.71058962A>C (hg19) ; chr2:g.70831831A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831831A>C , CM000664.2:g.70831831A>C	GRCh38
NC_000002.11:g.71058962A>C , CM000664.1:g.71058962A>C	GRCh37
NC_000002.10:g.70912470A>C	NCBI36
NG_033914.1:g.8993T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-12T>G MANE Select	ENSP00000386378.3:n.718-12T>G
ENST00000410009.4:c.718-12T>G	ENSP00000386378.3:n.718-12T>G
NM_015717.4:c.718-12T>G	NP_056532.4:n.718-12T>G
XM_011532874.1:c.718-12T>G	XP_011531176.1:n.718-12T>G
XM_011532875.1:c.718-12T>G	XP_011531177.1:n.718-12T>G
XM_011532876.1:c.718-12T>G	XP_011531178.1:n.718-12T>G
XM_011532875.2:c.718-12T>G	XP_011531177.1:n.718-12T>G
XM_011532876.2:c.718-12T>G	XP_011531178.1:n.718-12T>G
NM_015717.5:c.718-12T>G MANE Select	NP_056532.4:n.718-12T>G