Canonical Allele Identifier: CA892614215
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1180206932
gnomAD v4: 2-70831648-C-T
MyVariant Identifiers: chr2:g.70831648C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831648C>T , CM000664.2:g.70831648C>T GRCh38
NC_000002.11:g.71058779C>T , CM000664.1:g.71058779C>T GRCh37
NC_000002.10:g.70912287C>T NCBI36
NG_033914.1:g.9176G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+53G>A MANE Select ENSP00000386378.3:n.836+53G>A
ENST00000410009.4:c.836+53G>A ENSP00000386378.3:n.836+53G>A
NM_015717.4:c.836+53G>A NP_056532.4:n.836+53G>A
XM_011532874.1:c.836+53G>A XP_011531176.1:n.836+53G>A
XM_011532875.1:c.836+53G>A XP_011531177.1:n.836+53G>A
XM_011532876.1:c.836+53G>A XP_011531178.1:n.836+53G>A
XM_011532875.2:c.836+53G>A XP_011531177.1:n.836+53G>A
XM_011532876.2:c.836+53G>A XP_011531178.1:n.836+53G>A
NM_015717.5:c.836+53G>A MANE Select NP_056532.4:n.836+53G>A
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