Canonical Allele Identifier: CA9426131
Gene: IFNL3 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.39245004C>G
GRCh37 chr19:g.39735644C>G
gnomAD v2:
19:39735644 C / G
gnomAD v3:
19:39245004 C / G
gnomAD v4:
chr19-39245004-C-G
Joint Max Group AF 0.60241942 (AFR)
Genomes Max Group AF 0.59824049 (AFR)
Exomes Max Group AF 0.60326515 (AFR)
dbSNP:
28416813
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39245004C>G , CM000681.2:g.39245004C>G GRCh38
NC_000019.9:g.39735644C>G , CM000681.1:g.39735644C>G GRCh37
NC_000019.8:g.44427484C>G NCBI36
NG_042193.1:g.4968G>C
NG_055295.1:g.8853G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000613087.5:c.11-35G>C ENSP00000481633.1:n.11-35G>C
ENST00000413851.3:c.-37G>C MANE Select ENSP00000409000.2:n.-37G>C
ENST00000413851.2:c.-37G>C ENSP00000409000.2:n.-37G>C
ENST00000613087.4:c.11-35G>C ENSP00000481633.1:n.11-35G>C
XM_005258765.3:c.11-35G>C XP_005258822.1:n.11-35G>C
XM_011526757.1:c.11-35G>C XP_011525059.1:n.11-35G>C
NM_001346937.1:c.11-35G>C NP_001333866.1:n.11-35G>C
NM_172139.3:c.-37G>C NP_742151.2:n.-37G>C
NM_172139.4:c.-37G>C MANE Select NP_742151.2:n.-37G>C
NM_001346937.2:c.11-35G>C NP_001333866.1:n.11-35G>C
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