Canonical Allele Identifier: CA347179612
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1677482004
MyVariant Identifiers: chr2:g.71058947A>G (hg19) chr2:g.70831816A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831816A>G , CM000664.2:g.70831816A>G GRCh38
NC_000002.11:g.71058947A>G , CM000664.1:g.71058947A>G GRCh37
NC_000002.10:g.70912455A>G NCBI36
NG_033914.1:g.9008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.721T>C MANE Select ENSP00000386378.3:p.Phe241Leu
ENST00000410009.4:c.721T>C ENSP00000386378.3:p.Phe241Leu
NM_015717.4:c.721T>C NP_056532.4:p.Phe241Leu
XM_011532874.1:c.721T>C XP_011531176.1:p.Phe241Leu
XM_011532875.1:c.721T>C XP_011531177.1:p.Phe241Leu
XM_011532876.1:c.721T>C XP_011531178.1:p.Phe241Leu
XM_011532875.2:c.721T>C XP_011531177.1:p.Phe241Leu
XM_011532876.2:c.721T>C XP_011531178.1:p.Phe241Leu
NM_015717.5:c.721T>C MANE Select NP_056532.4:p.Phe241Leu
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