Canonical Allele Identifier: CA2659495046
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831958-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831958T>C , CM000664.2:g.70831958T>C GRCh38
NC_000002.11:g.71059089T>C , CM000664.1:g.71059089T>C GRCh37
NC_000002.10:g.70912597T>C NCBI36
NG_033914.1:g.8866A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-139A>G MANE Select ENSP00000386378.3:n.718-139A>G
ENST00000410009.4:c.718-139A>G ENSP00000386378.3:n.718-139A>G
NM_015717.4:c.718-139A>G NP_056532.4:n.718-139A>G
XM_011532874.1:c.718-139A>G XP_011531176.1:n.718-139A>G
XM_011532875.1:c.718-139A>G XP_011531177.1:n.718-139A>G
XM_011532876.1:c.718-139A>G XP_011531178.1:n.718-139A>G
XM_011532875.2:c.718-139A>G XP_011531177.1:n.718-139A>G
XM_011532876.2:c.718-139A>G XP_011531178.1:n.718-139A>G
NM_015717.5:c.718-139A>G MANE Select NP_056532.4:n.718-139A>G
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