Canonical Allele Identifier: CA892614207
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1250924812
gnomAD v4: 2-70831638-C-G
MyVariant Identifiers: chr2:g.70831638C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831638C>G , CM000664.2:g.70831638C>G GRCh38
NC_000002.11:g.71058769C>G , CM000664.1:g.71058769C>G GRCh37
NC_000002.10:g.70912277C>G NCBI36
NG_033914.1:g.9186G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.836+63G>C MANE Select ENSP00000386378.3:n.836+63G>C
ENST00000410009.4:c.836+63G>C ENSP00000386378.3:n.836+63G>C
NM_015717.4:c.836+63G>C NP_056532.4:n.836+63G>C
XM_011532874.1:c.836+63G>C XP_011531176.1:n.836+63G>C
XM_011532875.1:c.836+63G>C XP_011531177.1:n.836+63G>C
XM_011532876.1:c.836+63G>C XP_011531178.1:n.836+63G>C
XM_011532875.2:c.836+63G>C XP_011531177.1:n.836+63G>C
XM_011532876.2:c.836+63G>C XP_011531178.1:n.836+63G>C
NM_015717.5:c.836+63G>C MANE Select NP_056532.4:n.836+63G>C
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