Canonical Allele Identifier: CA347179352
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831702-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831702T>A , CM000664.2:g.70831702T>A GRCh38
NC_000002.11:g.71058833T>A , CM000664.1:g.71058833T>A GRCh37
NC_000002.10:g.70912341T>A NCBI36
NG_033914.1:g.9122A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.835A>T MANE Select ENSP00000386378.3:p.Arg279Trp
ENST00000410009.4:c.835A>T ENSP00000386378.3:p.Arg279Trp
NM_015717.4:c.835A>T NP_056532.4:p.Arg279Trp
XM_011532874.1:c.835A>T XP_011531176.1:p.Arg279Trp
XM_011532875.1:c.835A>T XP_011531177.1:p.Arg279Trp
XM_011532876.1:c.835A>T XP_011531178.1:p.Arg279Trp
XM_011532875.2:c.835A>T XP_011531177.1:p.Arg279Trp
XM_011532876.2:c.835A>T XP_011531178.1:p.Arg279Trp
NM_015717.5:c.835A>T MANE Select NP_056532.4:p.Arg279Trp