Canonical Allele Identifier: CA2659494729

Gene: CD207

Linked Data

• gnomAD v4: 2-70831831-A-T

Genomic Alleles

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

Transcript Alleles

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