Canonical Allele Identifier: CA1700293
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs556671276
ExAC: 2:71058842 G / A
gnomAD v2: 2-71058842-G-A
gnomAD v3: 2-70831711-G-A
gnomAD v4: 2-70831711-G-A
MyVariant Identifiers: chr2:g.71058842G>A (hg19) chr2:g.70831711G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831711G>A , CM000664.2:g.70831711G>A GRCh38
NC_000002.11:g.71058842G>A , CM000664.1:g.71058842G>A GRCh37
NC_000002.10:g.70912350G>A NCBI36
NG_033914.1:g.9113C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.826C>T MANE Select ENSP00000386378.3:p.Gln276Ter
ENST00000410009.4:c.826C>T ENSP00000386378.3:p.Gln276Ter
NM_015717.4:c.826C>T NP_056532.4:p.Gln276Ter
XM_011532874.1:c.826C>T XP_011531176.1:p.Gln276Ter
XM_011532875.1:c.826C>T XP_011531177.1:p.Gln276Ter
XM_011532876.1:c.826C>T XP_011531178.1:p.Gln276Ter
XM_011532875.2:c.826C>T XP_011531177.1:p.Gln276Ter
XM_011532876.2:c.826C>T XP_011531178.1:p.Gln276Ter
NM_015717.5:c.826C>T MANE Select NP_056532.4:p.Gln276Ter
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