Canonical Allele Identifier: CA347179397
Gene: CD207 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831723A>C , CM000664.2:g.70831723A>C GRCh38
NC_000002.11:g.71058854A>C , CM000664.1:g.71058854A>C GRCh37
NC_000002.10:g.70912362A>C NCBI36
NG_033914.1:g.9101T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.814T>G MANE Select ENSP00000386378.3:p.Phe272Val
ENST00000410009.4:c.814T>G ENSP00000386378.3:p.Phe272Val
NM_015717.4:c.814T>G NP_056532.4:p.Phe272Val
XM_011532874.1:c.814T>G XP_011531176.1:p.Phe272Val
XM_011532875.1:c.814T>G XP_011531177.1:p.Phe272Val
XM_011532876.1:c.814T>G XP_011531178.1:p.Phe272Val
XM_011532875.2:c.814T>G XP_011531177.1:p.Phe272Val
XM_011532876.2:c.814T>G XP_011531178.1:p.Phe272Val
NM_015717.5:c.814T>G MANE Select NP_056532.4:p.Phe272Val