Canonical Allele Identifier: CA426673151
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831736-C-T
MyVariant Identifiers: chr2:g.71058867C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831736C>T , CM000664.2:g.70831736C>T GRCh38
NC_000002.11:g.71058867C>T , CM000664.1:g.71058867C>T GRCh37
NC_000002.10:g.70912375C>T NCBI36
NG_033914.1:g.9088G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.801G>A MANE Select ENSP00000386378.3:p.Val267=
ENST00000410009.4:c.801G>A ENSP00000386378.3:p.Val267=
NM_015717.4:c.801G>A NP_056532.4:p.Val267=
XM_011532874.1:c.801G>A XP_011531176.1:p.Val267=
XM_011532875.1:c.801G>A XP_011531177.1:p.Val267=
XM_011532876.1:c.801G>A XP_011531178.1:p.Val267=
XM_011532875.2:c.801G>A XP_011531177.1:p.Val267=
XM_011532876.2:c.801G>A XP_011531178.1:p.Val267=
NM_015717.5:c.801G>A MANE Select NP_056532.4:p.Val267=
Search 100 bp 5'
Search 100 bp 3'