Canonical Allele Identifier: CA2659494353
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831656-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831656T>A , CM000664.2:g.70831656T>A GRCh38
NC_000002.11:g.71058787T>A , CM000664.1:g.71058787T>A GRCh37
NC_000002.10:g.70912295T>A NCBI36
NG_033914.1:g.9168A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+45A>T MANE Select ENSP00000386378.3:n.836+45A>T
ENST00000410009.4:c.836+45A>T ENSP00000386378.3:n.836+45A>T
NM_015717.4:c.836+45A>T NP_056532.4:n.836+45A>T
XM_011532874.1:c.836+45A>T XP_011531176.1:n.836+45A>T
XM_011532875.1:c.836+45A>T XP_011531177.1:n.836+45A>T
XM_011532876.1:c.836+45A>T XP_011531178.1:n.836+45A>T
XM_011532875.2:c.836+45A>T XP_011531177.1:n.836+45A>T
XM_011532876.2:c.836+45A>T XP_011531178.1:n.836+45A>T
NM_015717.5:c.836+45A>T MANE Select NP_056532.4:n.836+45A>T