Canonical Allele Identifier: CA308187792
Gene: IFNL3 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.39245279C>T
GRCh37 chr19:g.39735919C>T
gnomAD v2:
19:39735919 C / T
gnomAD v3:
19:39245279 C / T
gnomAD v4:
chr19-39245279-C-T
Joint Max Group AF 0.33668395 (AMR)
Genomes Max Group AF 0.32024008 (AMR)
Exomes Max Group AF 0.34566042 (AMR)
dbSNP:
4803219
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39245279C>T , CM000681.2:g.39245279C>T GRCh38
NC_000019.9:g.39735919C>T , CM000681.1:g.39735919C>T GRCh37
NC_000019.8:g.44427759C>T NCBI36
NG_042193.1:g.4693G>A
NG_055295.1:g.8578G>A

Transcript Alleles

HGVS Amino-acid Change
XM_005258765.3:c.-202G>A XP_005258822.1:n.-202G>A
XM_011526757.1:c.-202G>A XP_011525059.1:n.-202G>A
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