Canonical Allele Identifier: CA347179486
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1350454924

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831759T>C , CM000664.2:g.70831759T>C GRCh38
NC_000002.11:g.71058890T>C , CM000664.1:g.71058890T>C GRCh37
NC_000002.10:g.70912398T>C NCBI36
NG_033914.1:g.9065A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.778A>G MANE Select ENSP00000386378.3:p.Met260Val
ENST00000410009.4:c.778A>G ENSP00000386378.3:p.Met260Val
NM_015717.4:c.778A>G NP_056532.4:p.Met260Val
XM_011532874.1:c.778A>G XP_011531176.1:p.Met260Val
XM_011532875.1:c.778A>G XP_011531177.1:p.Met260Val
XM_011532876.1:c.778A>G XP_011531178.1:p.Met260Val
XM_011532875.2:c.778A>G XP_011531177.1:p.Met260Val
XM_011532876.2:c.778A>G XP_011531178.1:p.Met260Val
NM_015717.5:c.778A>G MANE Select NP_056532.4:p.Met260Val