Canonical Allele Identifier: CA426673155
Gene: CD207 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.71058873G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831742G>C , CM000664.2:g.70831742G>C GRCh38
NC_000002.11:g.71058873G>C , CM000664.1:g.71058873G>C GRCh37
NC_000002.10:g.70912381G>C NCBI36
NG_033914.1:g.9082C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.795C>G MANE Select ENSP00000386378.3:p.Ser265=
ENST00000410009.4:c.795C>G ENSP00000386378.3:p.Ser265=
NM_015717.4:c.795C>G NP_056532.4:p.Ser265=
XM_011532874.1:c.795C>G XP_011531176.1:p.Ser265=
XM_011532875.1:c.795C>G XP_011531177.1:p.Ser265=
XM_011532876.1:c.795C>G XP_011531178.1:p.Ser265=
XM_011532875.2:c.795C>G XP_011531177.1:p.Ser265=
XM_011532876.2:c.795C>G XP_011531178.1:p.Ser265=
NM_015717.5:c.795C>G MANE Select NP_056532.4:p.Ser265=
Search 100 bp 5'
Search 100 bp 3'