Canonical Allele Identifier: CA7974257
Gene: IL4R HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2234895

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.27346606C>T , CM000678.2:g.27346606C>T GRCh38
NC_000016.9:g.27357927C>T , CM000678.1:g.27357927C>T GRCh37
NC_000016.8:g.27265428C>T NCBI36
NG_012086.1:g.37677C>T

Transcript Alleles

HGVS Amino-acid change
NM_000418.3:c.501C>T VV NP_000409.1:p.Asn167=
NM_001257406.1:c.501C>T VV NP_001244335.1:p.Asn167=
NM_001257407.1:c.456C>T VV NP_001244336.1:p.Asn152=
NM_001257997.1:c.26C>T VV NP_001244926.1:p.Thr9Met
XM_011545825.1:c.501C>T XP_011544127.1:p.Asn167=
XM_011545826.1:c.501C>T XP_011544128.1:p.Asn167=
XM_011545827.1:c.501C>T XP_011544129.1:p.Asn167=
XM_011545828.1:c.234C>T XP_011544130.1:p.Asn78=
XM_011545829.1:c.216+1586C>T XP_011544131.1:p.=
XM_011545830.1:c.216+1586C>T XP_011544132.1:p.=
XM_011545831.1:c.216+1586C>T XP_011544133.1:p.=
XM_011545832.1:c.216+1586C>T XP_011544134.1:p.=
XM_011545833.1:c.216+1586C>T XP_011544135.1:p.=
XM_011545834.1:c.90+1586C>T XP_011544136.1:p.=
XM_011545826.2:c.501C>T XP_011544128.1:p.Asn167=
XM_011545827.2:c.501C>T XP_011544129.1:p.Asn167=
XM_011545828.2:c.234C>T XP_011544130.1:p.Asn78=
XM_011545830.2:c.216+1586C>T XP_011544132.1:p.=
XM_011545833.2:c.216+1586C>T XP_011544135.1:p.=
XM_011545834.2:c.90+1586C>T XP_011544136.1:p.=
XM_017023211.1:c.501C>T XP_016878700.1:p.Asn167=
NM_000418.4:c.501C>T VV MANE Preferred NP_000409.1:p.Asn167=
ENST00000170630.6:n.456C>T ENSP00000170630.3:p.Asn152=
ENST00000395762.6:c.501C>T ENSP00000379111.2:p.Asn167=
ENST00000543915.6:c.501C>T ENSP00000441667.2:p.Asn167=
ENST00000565696.1:n.521C>T
ENST00000566318.5:c.361+1586C>T ENSP00000456248.1:p.=
ENST00000568746.5:c.*544C>T ENSP00000455714.1:p.=