Canonical Allele Identifier: CA1032026329
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1677476319
gnomAD v3: 2-70831656-T-C
gnomAD v4: 2-70831656-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831656T>C , CM000664.2:g.70831656T>C GRCh38
NC_000002.11:g.71058787T>C , CM000664.1:g.71058787T>C GRCh37
NC_000002.10:g.70912295T>C NCBI36
NG_033914.1:g.9168A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+45A>G MANE Select ENSP00000386378.3:n.836+45A>G
ENST00000410009.4:c.836+45A>G ENSP00000386378.3:n.836+45A>G
NM_015717.4:c.836+45A>G NP_056532.4:n.836+45A>G
XM_011532874.1:c.836+45A>G XP_011531176.1:n.836+45A>G
XM_011532875.1:c.836+45A>G XP_011531177.1:n.836+45A>G
XM_011532876.1:c.836+45A>G XP_011531178.1:n.836+45A>G
XM_011532875.2:c.836+45A>G XP_011531177.1:n.836+45A>G
XM_011532876.2:c.836+45A>G XP_011531178.1:n.836+45A>G
NM_015717.5:c.836+45A>G MANE Select NP_056532.4:n.836+45A>G