Canonical Allele Identifier: CA347179378
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1677478318
gnomAD v4: 2-70831715-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831715C>G , CM000664.2:g.70831715C>G GRCh38
NC_000002.11:g.71058846C>G , CM000664.1:g.71058846C>G GRCh37
NC_000002.10:g.70912354C>G NCBI36
NG_033914.1:g.9109G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.822G>C MANE Select ENSP00000386378.3:p.Lys274Asn
ENST00000410009.4:c.822G>C ENSP00000386378.3:p.Lys274Asn
NM_015717.4:c.822G>C NP_056532.4:p.Lys274Asn
XM_011532874.1:c.822G>C XP_011531176.1:p.Lys274Asn
XM_011532875.1:c.822G>C XP_011531177.1:p.Lys274Asn
XM_011532876.1:c.822G>C XP_011531178.1:p.Lys274Asn
XM_011532875.2:c.822G>C XP_011531177.1:p.Lys274Asn
XM_011532876.2:c.822G>C XP_011531178.1:p.Lys274Asn
NM_015717.5:c.822G>C MANE Select NP_056532.4:p.Lys274Asn