Canonical Allele Identifier: CA14634122
Gene: CD209 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.7740242G>A
GRCh37 chr19:g.7805128G>A
gnomAD v2:
19:7805128 G / A
gnomAD v3:
19:7740242 G / A
gnomAD v4:
chr19-7740242-G-A
Joint Max Group AF 0.87281222 (NFE)
Genomes Max Group AF 0.86903041 (NFE)
Exomes Max Group AF 0.87267815 (NFE)
dbSNP:
4804800
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7740242G>A , CM000681.2:g.7740242G>A GRCh38
NC_000019.9:g.7805128G>A , CM000681.1:g.7805128G>A GRCh37
NC_000019.8:g.7711128G>A NCBI36
NG_012167.1:g.12337C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315599.12:c.*2797C>T MANE Select ENSP00000315477.6:n.*2797C>T
ENST00000676543.1:c.70+5276C>T ENSP00000503143.1:n.70+5276C>T
ENST00000678003.1:c.476+1325C>T ENSP00000504497.1:n.476+1325C>T
ENST00000678227.1:n.579+1325C>T
ENST00000678780.1:c.1971+1325C>T ENSP00000503751.1:n.1971+1325C>T
ENST00000315599.11:c.*2797C>T ENSP00000315477.6:n.*2797C>T
NM_001144893.1:c.*2797C>T NP_001138365.1:n.*2797C>T
NM_001144894.1:c.*2797C>T NP_001138366.1:n.*2797C>T
NM_001144895.1:c.*2797C>T NP_001138367.1:n.*2797C>T
NM_001144896.1:c.*2797C>T NP_001138368.1:n.*2797C>T
NM_001144897.1:c.*2797C>T NP_001138369.1:n.*2797C>T
NM_001144899.1:c.*2797C>T NP_001138371.1:n.*2797C>T
NM_021155.3:c.*2797C>T NP_066978.1:n.*2797C>T
NR_026692.1:n.4179C>T
XM_005272472.3:c.*2797C>T XP_005272529.1:n.*2797C>T
XM_005272472.4:c.*2797C>T XP_005272529.1:n.*2797C>T
NM_021155.4:c.*2797C>T MANE Select NP_066978.1:n.*2797C>T
NM_001144893.2:c.*2797C>T NP_001138365.1:n.*2797C>T
NM_001144894.2:c.*2797C>T NP_001138366.1:n.*2797C>T
NM_001144895.2:c.*2797C>T NP_001138367.1:n.*2797C>T
NM_001144896.2:c.*2797C>T NP_001138368.1:n.*2797C>T
NM_001144897.2:c.*2797C>T NP_001138369.1:n.*2797C>T
NM_001144899.2:c.*2797C>T NP_001138371.1:n.*2797C>T
NR_026692.2:n.4135C>T
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