Canonical Allele Identifier: CA892614145
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1250276063
MyVariant Identifiers: chr2:g.70831573G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831573G>T , CM000664.2:g.70831573G>T GRCh38
NC_000002.11:g.71058704G>T , CM000664.1:g.71058704G>T GRCh37
NC_000002.10:g.70912212G>T NCBI36
NG_033914.1:g.9251C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.836+128C>A MANE Select ENSP00000386378.3:n.836+128C>A
ENST00000410009.4:c.836+128C>A ENSP00000386378.3:n.836+128C>A
NM_015717.4:c.836+128C>A NP_056532.4:n.836+128C>A
XM_011532874.1:c.836+128C>A XP_011531176.1:n.836+128C>A
XM_011532875.1:c.836+128C>A XP_011531177.1:n.836+128C>A
XM_011532876.1:c.836+128C>A XP_011531178.1:n.836+128C>A
XM_011532875.2:c.836+128C>A XP_011531177.1:n.836+128C>A
XM_011532876.2:c.836+128C>A XP_011531178.1:n.836+128C>A
NM_015717.5:c.836+128C>A MANE Select NP_056532.4:n.836+128C>A
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