Canonical Allele Identifier: CA1700296
Gene: CD207 HGNC NCBI

Linked Data

ClinVar Variation Id: 3140431
ClinVar RCV Id: RCV004433320
dbSNP Id: rs374742141
ExAC: 2:71058859 G / A
gnomAD v2: 2-71058859-G-A
gnomAD v3: 2-70831728-G-A
gnomAD v4: 2-70831728-G-A
MyVariant Identifiers: chr2:g.71058859G>A (hg19) chr2:g.70831728G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831728G>A , CM000664.2:g.70831728G>A GRCh38
NC_000002.11:g.71058859G>A , CM000664.1:g.71058859G>A GRCh37
NC_000002.10:g.70912367G>A NCBI36
NG_033914.1:g.9096C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.809C>T MANE Select ENSP00000386378.3:p.Thr270Met
ENST00000410009.4:c.809C>T ENSP00000386378.3:p.Thr270Met
NM_015717.4:c.809C>T NP_056532.4:p.Thr270Met
XM_011532874.1:c.809C>T XP_011531176.1:p.Thr270Met
XM_011532875.1:c.809C>T XP_011531177.1:p.Thr270Met
XM_011532876.1:c.809C>T XP_011531178.1:p.Thr270Met
XM_011532875.2:c.809C>T XP_011531177.1:p.Thr270Met
XM_011532876.2:c.809C>T XP_011531178.1:p.Thr270Met
NM_015717.5:c.809C>T MANE Select NP_056532.4:p.Thr270Met
Search 100 bp 5'
Search 100 bp 3'