Canonical Allele Identifier: CA14217235
Gene: IL4R HGNC NCBI
MyVariant.info:
GRCh38 chr16:g.27364466A>G
GRCh37 chr16:g.27375787A>G
gnomAD v2:
16:27375787 A / G
gnomAD v3:
16:27364466 A / G
gnomAD v4:
chr16-27364466-A-G
Joint Max Group AF 0.55065754 (NFE)
Genomes Max Group AF 0.55077982 (NFE)
Exomes Max Group AF 0.41120479 (NFE)
dbSNP:
8832
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27364466A>G , CM000678.2:g.27364466A>G GRCh38
NC_000016.9:g.27375787A>G , CM000678.1:g.27375787A>G GRCh37
NC_000016.8:g.27283288A>G NCBI36
NG_012086.1:g.55537A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.*636A>G MANE Select ENSP00000379111.2:n.*636A>G
ENST00000170630.6:c.3069A>G ENSP00000170630.3:n.3069A>G
ENST00000395762.6:c.*636A>G ENSP00000379111.2:n.*636A>G
ENST00000543915.6:c.*636A>G ENSP00000441667.2:n.*636A>G
NM_000418.3:c.*636A>G NP_000409.1:n.*636A>G
NM_001257406.1:c.*636A>G NP_001244335.1:n.*636A>G
NM_001257407.1:c.*636A>G NP_001244336.1:n.*636A>G
NM_001257997.1:c.*636A>G NP_001244926.1:n.*636A>G
XM_005255308.2:c.*636A>G XP_005255365.1:n.*636A>G
XM_006721043.1:c.*636A>G XP_006721106.1:n.*636A>G
XM_011545825.1:c.*636A>G XP_011544127.1:n.*636A>G
XM_011545826.1:c.*636A>G XP_011544128.1:n.*636A>G
XM_011545827.1:c.*636A>G XP_011544129.1:n.*636A>G
XM_011545828.1:c.*636A>G XP_011544130.1:n.*636A>G
XM_011545829.1:c.*636A>G XP_011544131.1:n.*636A>G
XM_011545830.1:c.*636A>G XP_011544132.1:n.*636A>G
XM_011545831.1:c.*636A>G XP_011544133.1:n.*636A>G
XM_011545832.1:c.*636A>G XP_011544134.1:n.*636A>G
XM_011545833.1:c.*636A>G XP_011544135.1:n.*636A>G
XM_011545834.1:c.*636A>G XP_011544136.1:n.*636A>G
XM_011545826.2:c.*636A>G XP_011544128.1:n.*636A>G
XM_011545827.2:c.*636A>G XP_011544129.1:n.*636A>G
XM_011545828.2:c.*636A>G XP_011544130.1:n.*636A>G
XM_011545830.2:c.*636A>G XP_011544132.1:n.*636A>G
XM_011545833.2:c.*636A>G XP_011544135.1:n.*636A>G
XM_011545834.2:c.*636A>G XP_011544136.1:n.*636A>G
NM_000418.4:c.*636A>G MANE Select NP_000409.1:n.*636A>G
NM_001257406.2:c.*636A>G NP_001244335.1:n.*636A>G
NM_001257407.2:c.*636A>G NP_001244336.1:n.*636A>G
NM_001257997.2:c.*636A>G NP_001244926.1:n.*636A>G
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