Canonical Allele Identifier: CA892614684
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1469222645
gnomAD v3: 2-70831980-T-G
gnomAD v4: 2-70831980-T-G
MyVariant Identifiers: chr2:g.70831980T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831980T>G , CM000664.2:g.70831980T>G GRCh38
NC_000002.11:g.71059111T>G , CM000664.1:g.71059111T>G GRCh37
NC_000002.10:g.70912619T>G NCBI36
NG_033914.1:g.8844A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-161A>C MANE Select ENSP00000386378.3:n.718-161A>C
ENST00000410009.4:c.718-161A>C ENSP00000386378.3:n.718-161A>C
NM_015717.4:c.718-161A>C NP_056532.4:n.718-161A>C
XM_011532874.1:c.718-161A>C XP_011531176.1:n.718-161A>C
XM_011532875.1:c.718-161A>C XP_011531177.1:n.718-161A>C
XM_011532876.1:c.718-161A>C XP_011531178.1:n.718-161A>C
XM_011532875.2:c.718-161A>C XP_011531177.1:n.718-161A>C
XM_011532876.2:c.718-161A>C XP_011531178.1:n.718-161A>C
NM_015717.5:c.718-161A>C MANE Select NP_056532.4:n.718-161A>C
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