Canonical Allele Identifier: CA494470629
Gene: IL4R HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.27374089T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27362768T>G , CM000678.2:g.27362768T>G GRCh38
NC_000016.9:g.27374089T>G , CM000678.1:g.27374089T>G GRCh37
NC_000016.8:g.27281590T>G NCBI36
NG_012086.1:g.53839T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395762.7:c.1416T>G MANE Select ENSP00000379111.2:p.Pro472=
ENST00000170630.6:c.1371T>G ENSP00000170630.3:p.Pro457=
ENST00000395762.6:c.1416T>G ENSP00000379111.2:p.Pro472=
ENST00000543915.6:c.1416T>G ENSP00000441667.2:p.Pro472=
ENST00000565352.1:c.230-1335T>G ENSP00000461268.1:n.230-1335T>G
ENST00000568746.5:c.*1459T>G ENSP00000455714.1:n.*1459T>G
NM_000418.3:c.1416T>G NP_000409.1:p.Pro472=
NM_001257406.1:c.1416T>G NP_001244335.1:p.Pro472=
NM_001257407.1:c.1371T>G NP_001244336.1:p.Pro457=
NM_001257997.1:c.936T>G NP_001244926.1:p.Pro312=
XM_005255308.2:c.525T>G XP_005255365.1:p.Pro175=
XM_006721043.1:c.465T>G XP_006721106.1:p.Pro155=
XM_011545825.1:c.1416T>G XP_011544127.1:p.Pro472=
XM_011545826.1:c.1416T>G XP_011544128.1:p.Pro472=
XM_011545827.1:c.1416T>G XP_011544129.1:p.Pro472=
XM_011545828.1:c.1149T>G XP_011544130.1:p.Pro383=
XM_011545829.1:c.1119T>G XP_011544131.1:p.Pro373=
XM_011545830.1:c.1119T>G XP_011544132.1:p.Pro373=
XM_011545831.1:c.1119T>G XP_011544133.1:p.Pro373=
XM_011545832.1:c.1119T>G XP_011544134.1:p.Pro373=
XM_011545833.1:c.1119T>G XP_011544135.1:p.Pro373=
XM_011545834.1:c.993T>G XP_011544136.1:p.Pro331=
XM_011545826.2:c.1416T>G XP_011544128.1:p.Pro472=
XM_011545827.2:c.1416T>G XP_011544129.1:p.Pro472=
XM_011545828.2:c.1149T>G XP_011544130.1:p.Pro383=
XM_011545830.2:c.1119T>G XP_011544132.1:p.Pro373=
XM_011545833.2:c.1119T>G XP_011544135.1:p.Pro373=
XM_011545834.2:c.993T>G XP_011544136.1:p.Pro331=
XM_017023211.1:c.*451T>G XP_016878700.1:n.*451T>G
NM_000418.4:c.1416T>G MANE Select NP_000409.1:p.Pro472=
NM_001257406.2:c.1416T>G NP_001244335.1:p.Pro472=
NM_001257407.2:c.1371T>G NP_001244336.1:p.Pro457=
NM_001257997.2:c.936T>G NP_001244926.1:p.Pro312=