Canonical Allele Identifier: CA892614596
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1418072219
gnomAD v4: 2-70831843-G-C
MyVariant Identifiers: chr2:g.70831843G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831843G>C , CM000664.2:g.70831843G>C GRCh38
NC_000002.11:g.71058974G>C , CM000664.1:g.71058974G>C GRCh37
NC_000002.10:g.70912482G>C NCBI36
NG_033914.1:g.8981C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-24C>G MANE Select ENSP00000386378.3:n.718-24C>G
ENST00000410009.4:c.718-24C>G ENSP00000386378.3:n.718-24C>G
NM_015717.4:c.718-24C>G NP_056532.4:n.718-24C>G
XM_011532874.1:c.718-24C>G XP_011531176.1:n.718-24C>G
XM_011532875.1:c.718-24C>G XP_011531177.1:n.718-24C>G
XM_011532876.1:c.718-24C>G XP_011531178.1:n.718-24C>G
XM_011532875.2:c.718-24C>G XP_011531177.1:n.718-24C>G
XM_011532876.2:c.718-24C>G XP_011531178.1:n.718-24C>G
NM_015717.5:c.718-24C>G MANE Select NP_056532.4:n.718-24C>G